FDA Inspection
Gentian ASGentian AS – FDA Inspection, Mar 8, 2018
Record Details
This FDA Inspection record concerns Gentian AS, with an inspection on March 8, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Gentian AS
- Inspection Date
- March 8, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 29a02c6d-5b75-4812-9cbf-2d7510eed483
Inspection Facts
- Inspection number
- 1081876
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Gentian AS
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 20, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 21, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Gentian AS
- FDA Inspection 941234 - 2015-08-20
- FDA Inspection 791023 - 2012-06-21
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