FDA Inspection 607045 — Sigma-Aldrich Manufacturing LLC

Sigma-Aldrich Manufacturing LLC — FEI 1937990

The FDA completed an inspection of Sigma-Aldrich Manufacturing LLC on Sep 2, 2009 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). Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 2, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)

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