FDA Inspection 1077371 — PATHEON API, INC.

PATHEON API, INC. — FEI 3000717636

The FDA completed an inspection of PATHEON API, INC. on November 9, 2018 in Florence, SC. 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
November 9, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Florence, SC (United States)