FDA Inspection 721328 — MilliporeSigma

MilliporeSigma — FEI 1000138378

The FDA completed an inspection of MilliporeSigma on April 25, 2011 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 25, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)