9 September 1986
17 April 1986
COMMERCIAL ITEM DESCRIPTION
The General Services Administration has authorized the use of this Commercial Item Description.
Shall be Calcitonin-Salmon Injection.
Shall contain 200 I.U. of Calcitonin-Salmon per ml within the applicable assay limits for the injection.
Shall be suitable for Subcutaneous and Intramuscular use.
Workmanship. Injection shall be free from defects which detract from its appearance or impair its serviceability.
Unit. Vial (VI). One vial containing 2 ml, as specified, constitutes one unit.
Contractor certification. The contractor shall certify and maintain substantiating evidence that the product offered meets the salient characteristics of this Commercial Item Description, and that the product conforms to the producersí 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.
DISTRIBUTION STATEMENT A: Approved for public release; distribution is unlimited.
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