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483
•Hybrid Pharma LLC•November 9, 2023

FDA 483 - Hybrid Pharma LLC - November 09, 2023

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Record Details

An FDA inspection of Hybrid Pharma LLC, an outsourcing facility in Deerfield Beach, FL, revealed significant deficiencies in aseptic processing, laboratory controls, and record-keeping. Observations included contaminated HEPA filters, inadequate media fill simulations, unvalidated test methods, and the compounding of drug substances on the Category 2 list. Many of these issues were repeat observations from previous inspections, indicating persistent non-compliance.

Company
Hybrid Pharma LLC
Inspection Date
November 9, 2023
Product Type
Drugs
Office
Office of Medical Device and Radiological Health Division II
Person
  • Joanne E. King (Special Assistant)
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ID · d260439c-a40b-448d-8aa6-2a6123db72c8

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