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FDA Inspection
•M D Technologies, Inc.•April 1, 2026

M D Technologies, Inc. – FDA Inspection, Apr 1, 2026

Record Details

This FDA Inspection record concerns M D Technologies, Inc., with an inspection on April 1, 2026, issued by the Chicago District Office, covering medical devices & rad health.

Company
M D Technologies, Inc.
Inspection Date
April 1, 2026
Product Type
Medical Devices & Rad Health
Office
Chicago District Office
Person
  • Clifford F. Long (Issuing Officer)
View Company Profile

ID · 470eea7c-9b60-414f-8c6a-372abe2deaec

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1310572
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Medical Devices
Outcome
Form 483 issued, view the record

FDA Citations

2
  1. ISO 13485:2016 Clause 8.2.4Complaint handling procedures lack required elements
  2. ISO 13485:2016 Clause 8.2.2Complaint handling procedures lack required elements

Full citation text and observation details available on the Dashboard.

Other FDA inspections of M D Technologies, Inc.

3
DateClassificationOfficeProject area
August 8, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
October 24, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
November 3, 2010NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for M D Technologies, Inc.
  • FDA Inspection 1061468 - 2018-08-08
  • FDA Inspection 852600 - 2013-10-24
  • FDA Inspection 697495 - 2010-11-03

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