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FDA Inspection 976890 — Patheon Puerto Rico, Inc.

Patheon Puerto Rico, Inc. — FEI 3003113148

The FDA completed an inspection of Patheon Puerto Rico, Inc. on June 21, 2016 in Manati, PR. 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
June 21, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Manati, PR (United States)

Facility

Other inspections at this facility

  • 1174359 (VAI Tue Jul 12 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1106702 (VAI Tue Oct 15 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1053901 (VAI Thu May 31 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 941475 (VAI Thu Sep 03 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 891131 (VAI Mon Aug 11 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources