Company
GermanyDuerr Optronik Gmbh & Co. KG, Gechingen, Germany – FDA Inspections
Inspection records and compliance data for Duerr Optronik Gmbh & Co. KG in Gechingen. 1 FDA inspection on record, 1 Form 483, last inspected September 12, 2019.
Company Profile
This profile covers Duerr Optronik Gmbh & Co. KG based in Gechingen, Germany.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 0
- NAI
- 0
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
Inspected September 12, 2019.
Most cited issue areas
- Lack of or inadequate process validation1 inspection
- Software validation for automated processes1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| September 12, 2019 | Not classified | Medical Devices & Rad Health · Compliance: Devices | 1101905 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Duerr Optronik Gmbh & Co. KG
FEI Number
3001052305
Address
Gultlinger Str. 14, Gechingen, Germany
Country
Germany
ID: ceaee805-2f46-44ce-89fc-5096f8710479