FDA Inspection
Remington Medical, Inc.Remington Medical, Inc. – FDA Inspection, Nov 24, 2014
Record Details
This FDA Inspection record concerns Remington Medical, Inc., with an inspection on November 24, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Remington Medical, Inc.
- Inspection Date
- November 24, 2014
- Product Type
- Devices
View Company Profile
ID · c7570f55-51e4-4685-9199-8f387604dd09
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 904767
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.70(g)Equipment Installation, Placement, Specified Requirements
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Other FDA inspections of Remington Medical, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 11, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 6, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 17, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Remington Medical, Inc.
- FDA Inspection 1040873 - 2018-01-11
- FDA Inspection 790897 - 2012-06-06
- FDA Inspection 703174 - 2010-12-17
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