FDA Inspection
Medical Depot Inc.Medical Depot Inc. – FDA Inspection, Nov 8, 2010
Record Details
This FDA Inspection record concerns Medical Depot Inc., with an inspection on November 8, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medical Depot Inc.
- Inspection Date
- November 8, 2010
- Product Type
- Devices
View Company Profile
ID · 81e8196d-fad1-4b2a-ab6d-d9720b684909
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 698694
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
5- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Medical Depot Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 11, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 2, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 1, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 17, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medical Depot Inc.
- FDA Inspection 1081918 - 2018-07-11
- FDA Inspection 933166 - 2015-07-02
- FDA Inspection 816947 - 2013-02-01
- FDA Inspection 732614 - 2011-06-17
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