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 3007816026.
Observations1
Issue DateAugust 02, 2019
Status1 Related Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections1
Establishment Details
Firm
Vitalab Pharmacy, Inc. DBA Vasco Rx Specialty Pharmacy
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