A-A-53008
Examination. The leg holder pad shall be examined to determine compliance with all requirements contained in this specification.
Classification of defects. Examination shall be conducted in accordance with the classification of defects listed in table II. Examination shall not be restricted to the classified possible defects below.
TABLE II. Categories and Defects.
|
Categories |
Defects |
|
Major |
|
|
101 |
Pad foam not high density. |
|
102 |
Pad does not employ hook and pile type closure |
|
103 |
Outer layer of pad not closed cell foam. |
|
104 |
Foam not free of voids. |
Dimensional Examination. The pads shall be examined for defects in dimensions. Any dimension not within the specifications herein shall be classified as a defect.
Contractor certification. The contractor shall certify that the product offered meets the salient characteristics of this description and conforms to the producers’ own drawings, specifications, standards, and quality assurance practices. The Government reserves the right to require proof of such conformance prior to first delivery and thereafter as may be otherwise provided for under the provisions of the contract.
Regulatory requirements.
Federal Food, Drug and Cosmetic Act. If the product covered by this document has been determined by the U.S. Food and Drug Administration to be under its jurisdiction, the offeror/contractor shall comply, and be responsible for compliance by its subcontractors/suppliers, with the requirements of Federal Food, Drug and Cosmetic Act, as amended, and regulations promulgated thereunder. In addition, the offeror/contractor shall comply, and be responsible for compliance by its subcontractors/suppliers, with the requirements of all other applicable Federal, State, and local statutes, ordinances, and regulations.
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