Company
GermanyHGR Instrumente GmbH, Tuttlingen, Germany – FDA Inspections
Inspection records and compliance data for HGR Instrumente GmbH in Tuttlingen. 1 FDA inspection on record, 1 Form 483, last inspected January 24, 2019.
Company Profile
This profile covers HGR Instrumente GmbH based in Tuttlingen, Germany.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 0
- NAI
- 0
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
Inspected January 24, 2019.
Most cited issue areas
- Lack of or inadequate complaint procedures1 inspection
- Lack of or inadequate procedures1 inspection
- Lack of or inadequate process validation1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| January 24, 2019 | Not classified | Medical Devices & Rad Health · Compliance: Devices | 1078232 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
HGR Instrumente GmbH
FEI Number
3004028763
Address
Sattlerstr. 35, Tuttlingen, Germany
Country
Germany
ID: b4a4764f-5917-46c7-aa4e-010f107f53d0