Company
GermanyDimeda Instrumente GmbH, Tuttlingen, Germany – FDA Inspections
Inspection records and compliance data for Dimeda Instrumente GmbH in Tuttlingen. 3 FDA inspections on record, 1 Form 483, last inspected January 26, 2023.
Company Profile
This profile covers Dimeda Instrumente GmbH based in Tuttlingen, Germany.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 1
- NAI
- 1
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected December 2, 2010. Last inspected January 26, 2023.
Most cited issue areas
- Lack of or inadequate complaint procedures1 inspection
- Lack of System for Timely Submission of Reports1 inspection
- Supplier oversight1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| January 26, 2023 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1197575 |
| August 30, 2018 | Not classified | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1064785 |
| December 2, 2010 | VAI | Medical Devices & Rad Health · Compliance: Devices | 702557 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Dimeda Instrumente GmbH
FEI Number
3002806816
Address
Gansacker 54&58, Tuttlingen, Germany
Country
Germany
ID: 88ea56a6-c47b-47f8-b7c3-39895071a6f6