FDA Inspection 933850 — ACS Dobfar s.p.a.

ACS Dobfar s.p.a. — FEI 3009807048

The FDA completed an inspection of ACS Dobfar s.p.a. on July 10, 2015 in Agrate Brianza. 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
July 10, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Agrate Brianza (Italy)

Additional Details

Postmarket Adverse Drug Experience (PADE)