FDA Inspection
Medical Depot Inc.Medical Depot Inc. – FDA Inspection, Feb 1, 2013
Record Details
This FDA Inspection record concerns Medical Depot Inc., with an inspection on February 1, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medical Depot Inc.
- Inspection Date
- February 1, 2013
- Product Type
- Devices
View Company Profile
ID · 418e66a4-7de3-48e7-ab45-332b7a93d242
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 816947
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 803.18(e)MDR not evaluated per 820.198
- 21 CFR 820.40(a)Document review, approval by designated individual
- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.90(a)Nonconforming product, 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 |
| June 17, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 8, 2010 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Medical Depot Inc.
- FDA Inspection 1081918 - 2018-07-11
- FDA Inspection 933166 - 2015-07-02
- FDA Inspection 732614 - 2011-06-17
- FDA Inspection 698694 - 2010-11-08
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