Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3014539091.
Observations5
Issue DateNovember 29, 2018
StatusNo Warning Letter
Establishment TypeProducer of Non Sterile Drug Products
Related Inspections1
Establishment Details
Firm
Crawford's Professional Drugs, Inc. dba Diket's Professional Drugs, Inc.
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