Company
NorwayGentian AS, Moss, Norway – FDA Inspections
Inspection records and compliance data for Gentian AS in Moss. 3 FDA inspections on record, 1 Form 483, last inspected March 08, 2018.
Company Profile
This profile covers Gentian AS based in Moss, Norway.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 1
- NAI
- 1
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected June 21, 2012. Last inspected March 8, 2018.
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| March 8, 2018 | Not classified | Medical Devices & Rad Health | 1081876 |
| August 20, 2015 | VAI | Medical Devices & Rad Health · Compliance: Devices | 941234 |
| June 21, 2012 | NAI | Medical Devices & Rad Health · Compliance: Devices | 791023 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Gentian AS
FEI Number
3006801241
Address
Bjornasveien 5, Moss, Norway
Country
Norway
ID: cef2c04d-07a8-4e16-89d7-1e1a440bba96