FDA Inspection
Kem Medical Products CorpKem Medical Products Corp – FDA Inspection, Jul 21, 2022
Record Details
This FDA Inspection record concerns Kem Medical Products Corp, with an inspection on July 21, 2022, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kem Medical Products Corp
- Inspection Date
- July 21, 2022
- Product Type
- Devices
View Company Profile
ID · 50793f7c-11b8-4d87-a61a-7778ec2b683c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1175436
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Kem Medical Products Corp
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 15, 2020 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 21, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 10, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 27, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kem Medical Products Corp
- FDA Inspection 1115221 - 2020-01-15
- FDA Inspection 1003651 - 2017-02-21
- FDA Inspection 791042 - 2012-07-10
- FDA Inspection 623870 - 2009-10-27
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.