FDA Inspection
M D Technologies, Inc.M D Technologies, Inc. – FDA Inspection, Oct 24, 2013
Record Details
This FDA Inspection record concerns M D Technologies, Inc., with an inspection on October 24, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- M D Technologies, Inc.
- Inspection Date
- October 24, 2013
- Product Type
- Devices
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ID · b4399216-b46f-4cdd-a1fd-78276ceb37f2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 852600
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
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Other FDA inspections of M D Technologies, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 1, 2026 | NAI | Chicago District Office | Postmarket Assurance: Medical Devices |
| August 8, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 3, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for M D Technologies, Inc.
- FDA Inspection 1310572 - 2026-04-01
- FDA Inspection 1061468 - 2018-08-08
- FDA Inspection 697495 - 2010-11-03
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