FDA Inspection
MedTorque Inc.MedTorque Inc. – FDA Inspection, Nov 22, 2016
Record Details
This FDA Inspection record concerns MedTorque Inc., with an inspection on November 22, 2016, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · 47ae1082-f1d1-4223-bee6-442931536a94
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1001617
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
Full citation text and observation details available on the Dashboard.
Other FDA inspections of MedTorque Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 25, 2025 | NAI | Chicago District Office | Postmarket Assurance: Medical Devices |
| November 19, 2021 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 25, 2017 | Not classified | Chicago District Office |
Other documents for MedTorque Inc.
- FDA Inspection 1283758 - 2025-09-25
- FDA Inspection 1157272 - 2021-11-19
- FDA Inspection 1030403 - 2017-10-25
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.