FDA Inspection 1199206 — MedFact Engineering GmbH

MedFact Engineering GmbH — FEI 3008497357

The FDA completed an inspection of MedFact Engineering GmbH on February 16, 2023 in Lorrach. 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
February 16, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Lorrach (Germany)