Company
GermanyArthrex Gmbh, Munich, Germany – FDA Inspections
Inspection records and compliance data for Arthrex Gmbh in Munich. 4 FDA inspections on record, 1 Form 483, last inspected October 31, 2018.
Company Profile
This profile covers Arthrex Gmbh based in Munich, Germany.
FDA Inspection History
- FDA inspections
- 4
- OAI
- 0
- VAI
- 0
- NAI
- 1
- Unclassified
- 3
- Form 483s
- 1
- Warning letters
- 0
First inspected September 27, 2013. Last inspected October 31, 2018.
FDA inspections (4)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| October 31, 2018 | Not classified | Medical Devices & Rad Health | 1106560 |
| October 9, 2017 | Not classified | Medical Devices & Rad Health | 1045696 |
| October 12, 2016 | Not classified | Medical Devices & Rad Health | 996312 |
| September 27, 2013 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 853020 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Arthrex Gmbh
FEI Number
3002579136
Address
Erwin-Hielscher-Str. 9, Munich, Germany
Country
Germany
ID: efb315ef-4d91-48f2-a6a1-0848853befb7