# FDA Inspection 791023 - Gentian AS - June 21, 2012

Source: https://www.keypedia.com/records/fda_inspections/gentian-as/b02f6714-962c-4f8e-b9d5-896cf22b2c20
Source feed: FDA_Inspections

> FDA Inspection 791023 for Gentian AS on June 21, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791023
- Company Name: Gentian AS
- Inspection Date: 2012-06-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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