FDA Inspection 1062125 — Chiesi USA, Inc.

Chiesi USA, Inc. — FEI 3006389494

The FDA completed an inspection of Chiesi USA, Inc. on June 15, 2018 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
June 15, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cary, NC (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)