FDA Inspection 659477 — Ames Goldsmith Corporation

Ames Goldsmith Corporation — FEI 1317366

The FDA completed an inspection of Ames Goldsmith Corporation on Apr 26, 2010 in Glens Falls, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 26, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Glens Falls, NY (United States)

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