# COMECER NETHERLANDS B.V. – FDA Inspection, Sep 8, 2022

Source: https://www.keypedia.com/records/fda_inspections/comecer-netherlands-bv/d7e4d2f7-f9c0-4709-826a-7aea0f0d1a71
Source feed: FDA_Inspections

> FDA inspection 1180920 of COMECER NETHERLANDS B.V., September 08, 2022. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180920
- Company Name: COMECER NETHERLANDS B.V.
- Inspection Date: 2022-09-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1069729 - 2018-04-19](https://www.keypedia.com/records/fda_inspections/comecer-netherlands-bv/694bdea9-2a11-46ba-bab0-70748187227a)

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