Company
GermanyRichard Wolf GmbH, Knittlingen, Germany – FDA Inspections
Inspection records and compliance data for Richard Wolf GmbH in Knittlingen. 5 FDA inspections on record (1 OAI), 1 Form 483, last inspected March 06, 2024.
Company Profile
This profile covers Richard Wolf GmbH based in Knittlingen, Germany.
FDA Inspection History
- FDA inspections
- 5
- OAI
- 1
- VAI
- 2
- NAI
- 1
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected June 10, 2010. Last inspected March 6, 2024.
Most cited issue areas
- Records, DHR {see also 820.184(e)}2 inspections
FDA inspections (5)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| March 6, 2024 | Not classified | Medical Devices & Rad Health · Compliance: Devices | 1231967 |
| October 20, 2022 | OAI | Medical Devices & Rad Health · Compliance: Devices | 1198730 |
| September 10, 2019 | VAI | Medical Devices & Rad Health · Radiation Control and Health Safety Act | 1106603 |
| August 29, 2014 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 896070 |
| June 10, 2010 | VAI | Medical Devices & Rad Health · Compliance: Devices | 665977 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Richard Wolf GmbH
FEI Number
3002808001
Address
Pforzheimer Str. 32, Knittlingen, Germany
Country
Germany
ID: 1ee7dffb-7df4-4519-886b-b7124dbc3ac8