FDA Inspection 916186 — Allergan Industrie SAS

Allergan Industrie SAS — FEI 3005113652

The FDA completed an inspection of Allergan Industrie SAS on January 29, 2015 in Pringy. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 29, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Pringy (France)

Additional Details

Postmarket Audit Inspections