FDA Inspection 877817 — Alfasigma USA, Inc.

Alfasigma USA, Inc. — FEI 3011104045

The FDA completed an inspection of Alfasigma USA, Inc. on May 8, 2014 in Shreveport, LA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 8, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shreveport, LA (United States)

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