FDA Inspection 951425 — AGC, Inc.

AGC, Inc. — FEI 3003282601

The FDA completed an inspection of AGC, Inc. on December 4, 2015 in Ichihara. 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
December 4, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ichihara (Japan)