FDA Inspection 607472 — Sigma-Aldrich Mfg LLC

Sigma-Aldrich Mfg LLC — FEI 1937991

The FDA completed an inspection of Sigma-Aldrich Mfg 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)