Company
GermanyOD-OS GmbH, Teltow, Germany – FDA Inspections
Inspection records and compliance data for OD-OS GmbH in Teltow. 4 FDA inspections on record, 1 Form 483, last inspected May 21, 2026.
Company Profile
This profile covers OD-OS GmbH based in Teltow, Germany.
FDA Inspection History
- FDA inspections
- 4
- OAI
- 0
- VAI
- 1
- NAI
- 1
- Unclassified
- 2
- Form 483s
- 1
- Warning letters
- 0
First inspected January 29, 2015. Last inspected May 21, 2026.
Most cited issue areas
- Design verification - documentation1 inspection
FDA inspections (4)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| May 21, 2026 | Not classified | Medical Devices & Rad Health | 1323728 |
| November 29, 2023 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1225993 |
| November 30, 2017 | Not classified | Medical Devices & Rad Health · Radiation Control and Health Safety Act | 1036165 |
| January 29, 2015 | VAI | Medical Devices & Rad Health · Compliance: Devices | 914693 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
OD-OS GmbH
FEI Number
3008252121
Address
Warthestr. 21, Teltow, Germany
Country
Germany
ID: ca319f54-b75a-4b09-80cf-1743766b61a1