FDA Inspection 996283 — MeKo Manufacturing E.K.
The FDA completed an inspection of MeKo Manufacturing E.K. on Jan 6, 2017 in Sarstedt. 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
- Jan 6, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sarstedt (Germany)