FDA Inspection 961490 — MeKo Manufacturing E.K.
The FDA completed an inspection of MeKo Manufacturing E.K. on Feb 11, 2016 in Sarstedt. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection details
- Classification
- Official Action Indicated (OAI)
- End Date
- Feb 11, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sarstedt (Germany)