# FDA Inspection 817910 - GC Europe N.V. - February 05, 2013

Source: https://www.keypedia.com/records/fda_inspections/gc-europe-nv/b4a89db9-7b31-442d-8a94-5b6883a0e749
Source feed: FDA_Inspections

> FDA Inspection 817910 for GC Europe N.V. on February 05, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 817910
- Company Name: GC Europe N.V.
- Inspection Date: 2013-02-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 817910 - 2013-02-05](https://www.keypedia.com/records/fda_inspections/gc-europe-nv/23d651bc-5bd5-401d-83c5-3728dd493e35)
- [FDA Inspection 546188 - 2008-10-29](https://www.keypedia.com/records/fda_inspections/gc-europe-nv/67415c92-a8ee-4ba9-be8d-9df190afe3d4)

Company: https://www.keypedia.com/companies/gc-europe-nv/f51637f6-59e6-4cb4-bd3c-16a05af68925

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