FDA Inspection
Medtec Applications, Inc.Medtec Applications, Inc. – FDA Inspection, May 10, 2010
Record Details
This FDA Inspection record concerns Medtec Applications, Inc., with an inspection on May 10, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medtec Applications, Inc.
- Inspection Date
- May 10, 2010
- Product Type
- Devices
View Company Profile
ID · 2761a43a-7ca3-4ca5-b485-12fc83dc37c5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 669533
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.184Lack of or inadequate DHR procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Medtec Applications, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| April 11, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 19, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 25, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 13, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medtec Applications, Inc.
- FDA Inspection 1205006 - 2023-04-11
- FDA Inspection 1078407 - 2018-12-19
- FDA Inspection 939441 - 2015-08-25
- FDA Inspection 806868 - 2012-11-13
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.