# FDA Inspection 1069729 - COMECER NETHERLANDS B.V. - April 19, 2018

Source: https://www.keypedia.com/records/fda_inspections/comecer-netherlands-bv/694bdea9-2a11-46ba-bab0-70748187227a
Source feed: FDA_Inspections

> FDA Inspection 1069729 for COMECER NETHERLANDS B.V. on April 19, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1069729
- Company Name: COMECER NETHERLANDS B.V.
- Inspection Date: 2018-04-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1180920 - 2022-09-08](https://www.keypedia.com/records/fda_inspections/comecer-netherlands-bv/d7e4d2f7-f9c0-4709-826a-7aea0f0d1a71)

Company: https://www.keypedia.com/companies/comecer-netherlands-bv/54b35b19-f301-4d90-8312-102399e292a0

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7