FDA Inspection 1219448 — Prodimed

Prodimed — FEI 3002807433

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.