FDA Inspection 1069729 — COMECER NETHERLANDS B.V.
The FDA completed an inspection of COMECER NETHERLANDS B.V. on Apr 19, 2018 in Joure. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 19, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Joure (Netherlands)