FDA Inspection 953970 — Hamari PFST, Ltd.

Hamari PFST, Ltd. — FEI 3002808528

The FDA completed an inspection of Hamari PFST, Ltd. on November 20, 2015 in Yonezawa. 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 20, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Yonezawa (Japan)