# FDA Inspection 941234 - Gentian AS - August 20, 2015

Source: https://www.keypedia.com/records/fda_inspections/gentian-as/a598038b-2059-43bf-b9f0-876aa144e242
Source feed: FDA_Inspections

> FDA Inspection 941234 for Gentian AS on August 20, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 941234
- Company Name: Gentian AS
- Inspection Date: 2015-08-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 941234 - 2015-08-20](https://www.keypedia.com/records/fda_inspections/gentian-as/f115c21a-3c60-457a-a863-64fca1442639)
- [FDA Inspection 791023 - 2012-06-21](https://www.keypedia.com/records/fda_inspections/gentian-as/b02f6714-962c-4f8e-b9d5-896cf22b2c20)
- [FDA Inspection 791023 - 2012-06-21](https://www.keypedia.com/records/fda_inspections/gentian-as/c289f584-3198-4750-a4f3-8a6a69b9446e)

Company: https://www.keypedia.com/companies/gentian-as/cef2c04d-07a8-4e16-89d7-1e1a440bba96

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