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FDA Inspection 720755 — Ames Goldsmith Corporation

Ames Goldsmith Corporation — FEI 1317366

The FDA completed an inspection of Ames Goldsmith Corporation on April 21, 2011 in Glens Falls, NY. 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
April 21, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Glens Falls, NY (United States)

Facility

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FDA data resources