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FDA Inspection 1010226 — Sigma-Aldrich Manufacturing LLC

Sigma-Aldrich Manufacturing LLC — FEI 1937990

The FDA completed an inspection of Sigma-Aldrich Manufacturing LLC on March 10, 2017 in Saint Louis, MO. 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
March 10, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Louis, MO (United States)

Facility

Other inspections at this facility

  • 1269843 (VAI Mon Apr 28 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1083240 (VAI Wed Feb 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 857968 (NAI Mon Dec 09 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 786662 (VAI Mon Jun 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 728049 (VAI Tue Apr 19 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources