FDA Inspection 1106702 — Patheon Puerto Rico, Inc.

Patheon Puerto Rico, Inc. — FEI 3003113148

The FDA completed an inspection of Patheon Puerto Rico, Inc. on October 15, 2019 in Manati, PR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 15, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Manati, PR (United States)

Citations

IDCFRDescription
135821 CFR 211.100(b)SOPs not followed / documented
202721 CFR 211.192Investigations of discrepancies, failures