FDA Inspection
RAPID RELEASE TECHNOLOGIESRAPID RELEASE TECHNOLOGIES – FDA Inspection, Aug 24, 2017
Record Details
This FDA Inspection record concerns RAPID RELEASE TECHNOLOGIES, with an inspection on August 24, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ad65db70-3601-4683-9837-13ef827a9f9d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1024368
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of RAPID RELEASE TECHNOLOGIES
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 25, 2016 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 6, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for RAPID RELEASE TECHNOLOGIES
- FDA Inspection 977555 - 2016-05-25
- FDA Inspection 933507 - 2015-07-06
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