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" ... device comprising such shipment, delivery, or part is adulterated or misbranded within the meaning of the act when so removed; or (2) Upon refusal by the operator of the establishment where such... "
Code of Federal Regulations: Containing a Codification of Documents of ... - 22. lappuse
2000
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Code of Federal Regulations: Containing a Codification of Documents of ...

1999 - 724 lapas
...article unless the device is labeled as required by §801.109. Subpart E — Other Exemptions §801.150 Medical devices; processing, labeling, or repacking....or to a contract sterilizer for sterilization, the Food and Drug Administration will initiate no regulatory action against the device as misbranded or...
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The Code of Federal Regulations of the United States of America

1999 - 724 lapas
...article unless the device is labeled as required by §801.109. Subpart E— Other Exemptions §801.150 Medical devices; processing, labeling, or repacking....a device as sterile at one establishment and then §801.405 ship such device in interstate commerce to another establishment or to a contract sterilizer...
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The Code of Federal Regulations of the United States of America

1993 - 630 lapas
...who requests them. (b) An exemption of a shipment or other delivery of a device under paragraph (a)U) of this section shall, at the beginning of the act...or to a contract sterilizer for sterilization, the Food and Drug Administration will initiate no regulatory action against the device as misbranded or...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2001 - 756 lapas
...requests them. (b) An exemption of a shipment or other delivery of a device under paragraph (a)(1) of this section shall, at the beginning of the act...or to a contract sterilizer for sterilization, the Food and Drug Administration will initiate no regulatory action against the device as misbranded or...
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The Code of Federal Regulations of the United States of America

1996 - 672 lapas
...removing such shipment or delivery, or any part thereof, from such establishment, become void ab initlo if the device comprising such shipment, delivery,...or to a contract sterilizer for sterilization, the Food and Drug Administration will initiate no regulatory action against the device as misbranded or...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1990 - 630 lapas
...void ab initio if the device comprising such shipment, delivery, or part is adulterated or mlsbranded within the meaning of the act when so removed. (c)...or to a contract sterilizer for sterilization, the Food and Drug Administration will initiate no regulatory action against the device as misbranded or...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1977 - 334 lapas
...paragraph (a) (2) . (d) An exemption of a shipment or other delivery of a device under paragraph (a) (2) of this section shall expire: (1) At the beginning...or to a contract sterilizer for sterilization, the Food and Drug Administration will initiate no regulatory action against the device as misbranded or...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1971 - 748 lapas
...the act when so removed; or (2) Upon refusal by the operator of the establishment where such drug or device is to be processed, labeled, or repacked, to...of the agreement, as required by such clause. (e) Except as provided in paragraphs (g) and (h) of this section, a shipment or other delivery of a drug...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1981 - 254 lapas
...of the act when so removed; or (2) Upon refusal by the operator of the establishment where such drug is to be processed, labeled, or repacked, to make...of the agreement, as required by such clause. (e) Except as provided in paragraphs (g) and (h) of this section, a shipment or other delivery of a drug...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1997 - 200 lapas
...of the act when so removed; or (2) Upon refusal by the operator of the establishment where such drug is to be processed, labeled, or repacked, to make...of the agreement, as required by such clause. (e) Except as provided in paragraphs (g) and (h) of this section, a shipment or other delivery of a drug...
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