FDA Inspection 1014313 — Prosoft Clinical

Prosoft Clinical — FEI 3013342045

The FDA completed an inspection of Prosoft Clinical on May 25, 2017 in Wayne, PA. 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
May 25, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Wayne, PA (United States)

Additional Details

Sponsor, Contract Research Organization