FDA Inspection 1219448 — Prodimed

Prodimed — FEI 3002807433

The FDA completed an inspection of Prodimed on August 24, 2023 in Neuilly En Thelle. 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
August 24, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Neuilly En Thelle (France)