FDA Inspection 933356 — Prosidyan Inc

Prosidyan Inc — FEI 3011015097

The FDA completed an inspection of Prosidyan Inc on June 23, 2015 in New Providence, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 23, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
New Providence, NJ (United States)