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FDA Inspection 941475 — Patheon Puerto Rico, Inc.

Patheon Puerto Rico, Inc. — FEI 3003113148

The FDA completed an inspection of Patheon Puerto Rico, Inc. on September 3, 2015 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
September 3, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Manati, PR (United States)

Facility

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  • 1053901 (VAI Thu May 31 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 976890 (VAI Tue Jun 21 2016 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