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A wholesale drug distributor shall prepare and follow a written policy for handling the recall of a drug due to
(1) a voluntary action on the part of the manufacturer;
(2) an order of the Food and Drug Administration, or of any other federal, state, or local government agency; or
(3) the replacement of an existing drug with an improved drug or new package design.
History: Eff. 1/16/98, Register 145
Authority: AS 08.80.005
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Last modified 7/05/2006