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FDA Inspection 607046 — Sigma-Aldrich Mfg LLC

Sigma-Aldrich Mfg LLC — FEI 1938173

The FDA completed an inspection of Sigma-Aldrich Mfg LLC on September 2, 2009 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: Devices.

Inspection Details

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

Facility

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FDA data resources