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" The requirement for inclusion of the ZIP Code shall apply only to consumer commodity labels developed or revised after the effective date of this section. In the case of nonconsumer packages, the ZIP Code shall appear on either the label or the labeling... "
Code of Federal Regulations: Containing a Codification of Documents of ... - 14. lappuse
2001
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Circular of the Bureau of Standards, 501. izdevums

United States. National Bureau of Standards - 1951
...directory or telephone directory. (c) Where a person manufactures, packs, or distributes a drug or d, statement, or other information appearing on the...not be considered to be complied with unless such each package of such drug or device was manufactured or packed or is to be distributed, if such statement...
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NBS Special Publication, 311. izdevums

1969
...developed or revised after July 1, 1968. If a person manufactures, packs, or distributes a commodity at a place other than his principal place of business,...place of business in lieu of the actual place where the commodity was manufactured or packed or is to be distributed, unless such statement would be misleading....
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The Code of Federal Regulations of the United States of America

1991
...of the Federal Pood, Drug, and Cosmetic Act (21 USC 321, 331, 351, 352, 357, 3601, 360J. 371, 374). SOURCE: 41 FR 6896, Feb. 13, 1976, unless otherwise...similar import in §§801.5, 801.119, and 801.122 refer to the objective intent of the persons legally responsible for the labeling of devices. The intent...
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The Code of Federal Regulations of the United States of America

1999
...for devices that contain natural rubber. AUTHORITY: 21 USC 321, 331, 351, 352, 360i, 360J, 371, 374. SOURCE: 41 FR 6896, Feb. 13, 1976, unless otherwise...similar import in §§801.5, 801.119, and 801.122 refer to the objective intent of the persons legally responsible for the labeling of devices. The intent...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1999
...that contain natural rubber. AUTHORITY: 21 USC 321. 331, 351, 352, 360i, 360j, 371, 374. SOURCE: 41 PR 6896. Feb. 13, 1976. unless otherwise noted. Subpart...similar import in §§801.5, 801.119, and 801.122 refer to the objective intent of the persons legally responsible for the labeling of devices. The intent...
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Code of Federal Regulations: Containing a ..., 21. izdevums,800-1299. daļas

1993
...Federal Food, Drug, and Cosmetic Act (21 USC 321. 331, 351, 352. 357, 3601, 360J, 371, 374). SOOTCE: 41 FR 6896. Feb. 13, 1976, unless otherwise noted....distributed, unless such statement would be misleading. § 801 .4 Meaning of "intended uses." The words "intended uses" or words of similar import in §§801.5,...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1977
...declaration of the name of the manufacturer, packer, or distributor shall be deemed to be satisfled, in the case of a corporation, only by the actual corporate...similar import in §§ 801.5, 801.119, and 801.122 refer to the objective intent of the persons legally responsible for the labeling of devices. The intent...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1996
...connection such person has with such device; such as, "Manufactured for Hi", "Distributed by HtH", or any other wording that expresses the facts. (d)...similar import in §§801.5, 801.119, and 801.122 refer to the objective Intent of the persons legally responsible for the labeling of devices. The intent...
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The Code of Federal Regulations of the United States of America

1974
...the labeling (including the invoice) . (e) If a person manufactures, packs, or distributes a drug or device at a place other than his principal place of...of business In lieu of the actual place where such drug or device was manufactured or packed or is to be distributed, unless such statement would be misleading....
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The Code of Federal Regulations of the United States of America

1972
...the labeling (including the invoice) . (e) If a person manufactures, packs, or distributes a drug or device at a place other than his principal place of...of business in lieu of the actual place where such drug or device was manufactured or packed or is to be distributed, unless such statement would be misleading....
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