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FDA Inspection 729681 — Patheon Puerto Rico, Inc.

Patheon Puerto Rico, Inc. — FEI 3003113148

The FDA completed an inspection of Patheon Puerto Rico, Inc. on June 15, 2011 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 15, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Manati, PR (United States)

Facility

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FDA data resources