FDA Inspection 923892 — Enraf-Nonius B.V.
The FDA completed an inspection of Enraf-Nonius B.V. on Apr 2, 2015 in Rotterdam. 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
- Apr 2, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Rotterdam (Netherlands)