FDA Inspection 918260 — Chiesi USA, Inc.

Chiesi USA, Inc. — FEI 3006389494

The FDA completed an inspection of Chiesi USA, Inc. on March 6, 2015 in Cary, NC. 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
March 6, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cary, NC (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)