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FDA Inspection 1282788 — Catalent Pharma Solutions, LLC

Catalent Pharma Solutions, LLC — FEI 1811396

The FDA completed an inspection of Catalent Pharma Solutions, LLC on January 30, 2026 in Saint Petersburg, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 30, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Petersburg, FL (United States)

Facility

Other inspections at this facility

  • 1229815 (NAI Thu May 30 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1229344 (NAI Thu Jan 25 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1210540 (VAI Fri Jul 21 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1101180 (VAI Wed Aug 28 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1080109 (VAI Fri Feb 22 2019 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources