FDA Inspection
JK Products & Services, IncJK Products & Services, Inc – FDA Inspection, Feb 10, 2012
Record Details
This FDA Inspection record concerns JK Products & Services, Inc, with an inspection on February 10, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- JK Products & Services, Inc
- Inspection Date
- February 10, 2012
- Product Type
- Devices
View Company Profile
ID · e0686061-c583-4aea-b719-d9c56b62aee9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 767474
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of JK Products & Services, Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 24, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 18, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 26, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 16, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for JK Products & Services, Inc
- FDA Inspection 1017825 - 2017-02-24
- FDA Inspection 900431 - 2014-09-18
- FDA Inspection 795416 - 2012-01-26
- FDA Inspection 685755 - 2010-09-16
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.