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FDA Inspection 975290 — Ames Goldsmith Corporation

Ames Goldsmith Corporation — FEI 1317366

The FDA completed an inspection of Ames Goldsmith Corporation on June 16, 2016 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
June 16, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Glens Falls, NY (United States)

Facility

Other inspections at this facility

  • 1271423 (VAI Thu May 22 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1121591 (VAI Fri Mar 06 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 885727 (VAI Wed Jun 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 813894 (VAI Thu Jan 10 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 764753 (VAI Thu Jan 26 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources