FDA Inspection 1012391 — LRE Medical GmbH
The FDA completed an inspection of LRE Medical GmbH on Feb 3, 2017 in Nordlingen. 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
- Feb 3, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Nordlingen (Germany)