FDA Inspection 1068032 — PEROUSE MEDICAL

PEROUSE MEDICAL — FEI 3006942524

The FDA completed an inspection of PEROUSE MEDICAL on Jul 18, 2018 in Ivry Le Temple. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 18, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Ivry Le Temple (France)