FDA Inspection 857970 — MilliporeSigma

MilliporeSigma — FEI 1000138378

The FDA completed an inspection of MilliporeSigma on December 9, 2013 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 9, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Louis, MO (United States)