FDA Inspection 1063787 — MedFact Engineering GmbH
The FDA completed an inspection of MedFact Engineering GmbH on July 25, 2018 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
- July 25, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lorrach (Germany)