FDA Inspection
M D Technologies, Inc.M D Technologies, Inc. – FDA Inspection, Aug 8, 2018
Record Details
This FDA Inspection record concerns M D Technologies, Inc., with an inspection on August 8, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c33299d9-a9bb-4637-9384-a09d7427751c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1061468
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
Full citation text and observation details available on the Dashboard.
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 |
| October 24, 2013 | 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 852600 - 2013-10-24
- FDA Inspection 697495 - 2010-11-03
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