FDA Inspection
RAPID RELEASE TECHNOLOGIESRAPID RELEASE TECHNOLOGIES – FDA Inspection, May 25, 2016
Record Details
This FDA Inspection record concerns RAPID RELEASE TECHNOLOGIES, with an inspection on May 25, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- RAPID RELEASE TECHNOLOGIES
- Inspection Date
- May 25, 2016
- Product Type
- Devices
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ID · fe323638-cfe5-48a5-a629-3fbf3191c1a3
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 977555
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of RAPID RELEASE TECHNOLOGIES
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 24, 2017 | VAI | 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 1024368 - 2017-08-24
- FDA Inspection 933507 - 2015-07-06
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