FDA Inspection 857968 — Sigma-Aldrich Manufacturing LLC

Sigma-Aldrich Manufacturing LLC — FEI 1937990

The FDA completed an inspection of Sigma-Aldrich Manufacturing LLC on Dec 9, 2013 in Saint Louis, MO. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 9, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)

Citations

IDCFRDescription
320421 CFR 820.40(b)Change records, content

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