FDA Inspection 1170976 — Merete GmbH

Merete GmbH — FEI 3002949614

The FDA completed an inspection of Merete GmbH on May 5, 2022 in Berlin. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 5, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Berlin (Germany)