FDA Inspection 739851 — AGC, Inc.

AGC, Inc. — FEI 3003282601

The FDA completed an inspection of AGC, Inc. on August 4, 2011 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
August 4, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ichihara (Japan)