FDA Inspection
RNK Products, IncRNK Products, Inc – FDA Inspection, Dec 14, 2017
Record Details
This FDA Inspection record concerns RNK Products, Inc, with an inspection on December 14, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 8e2856df-1e72-45b4-b0c4-4d12022f493a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1038933
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of RNK Products, Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 20, 2015 | 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 926848 - 2015-05-20
- FDA Inspection 769356 - 2012-02-23
- FDA Inspection 583442 - 2009-05-19
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