FDA Inspection
The Snore Reliever Company LLCThe Snore Reliever Company LLC – FDA Inspection, Feb 5, 2020
Record Details
This FDA Inspection record concerns The Snore Reliever Company LLC, with an inspection on February 5, 2020, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 5, 2020
- Product Type
- Devices
View Company Profile
ID · fae0c388-cf5d-4ba5-ad47-b91dff187c06
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1116928
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.90(a)Nonconforming product control
- 21 CFR 820.20(e)Quality System Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of The Snore Reliever Company LLC
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 29, 2024 | Not classified | Florida District Office | Compliance: Devices |
| October 25, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 12, 2012 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for The Snore Reliever Company LLC
- FDA Inspection 1248984 - 2024-08-29
- FDA Inspection 853465 - 2013-10-25
- FDA Inspection 786643 - 2012-06-12
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.