FDA Inspection
RNK Products, IncRNK Products, Inc – FDA Inspection, May 20, 2015
Record Details
This FDA Inspection record concerns RNK Products, Inc, with an inspection on May 20, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- RNK Products, Inc
- Inspection Date
- May 20, 2015
- Product Type
- Devices
View Company Profile
ID · f73a65ad-741e-41fc-9d87-2cdc9698ae34
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 926848
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of RNK Products, Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 14, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 23, 2012 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 19, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for RNK Products, Inc
- FDA Inspection 1038933 - 2017-12-14
- FDA Inspection 769356 - 2012-02-23
- FDA Inspection 583442 - 2009-05-19
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.