FDA Inspection 1220059 — Oertel Medical GmbH

Oertel Medical GmbH — FEI 3002809480

The FDA completed an inspection of Oertel Medical GmbH on August 31, 2023 in Tuttlingen. 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 31, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Tuttlingen (Germany)