FDA Inspection
A. R. Hinkel Company, Inc. dba R.A.FischerA. R. Hinkel Company, Inc. dba R.A.Fischer – FDA Inspection, Jan 24, 2020
Record Details
This FDA Inspection record concerns A. R. Hinkel Company, Inc. dba R.A.Fischer, with an inspection on January 24, 2020, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 24, 2020
- Product Type
- Devices
View Company Profile
ID · 7a50971a-9e9a-4201-94e1-007b74134971
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1115813
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of A. R. Hinkel Company, Inc. dba R.A.Fischer
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 13, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 6, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 18, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 27, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for A. R. Hinkel Company, Inc. dba R.A.Fischer
- FDA Inspection 1197738 - 2023-01-13
- FDA Inspection 971941 - 2016-06-06
- FDA Inspection 806461 - 2012-10-18
- FDA Inspection 695293 - 2010-10-27
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.