FDA Inspection
Contech Medical, Inc.Contech Medical, Inc. – FDA Inspection, Jun 10, 2013
Record Details
This FDA Inspection record concerns Contech Medical, Inc., with an inspection on June 10, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Contech Medical, Inc.
- Inspection Date
- June 10, 2013
- Product Type
- Devices
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ID · fb963dba-3482-4d0d-b0b8-eb218d3be7b5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 838112
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.60Identification procedures, Lack of or inadequate procedures
- 21 CFR 820.150Lack of or inadequate procedures for storage.
- 21 CFR 820.40(b)Document change records, maintained.
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Contech Medical, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 30, 2026 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 17, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 17, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 8, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 19, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Contech Medical, Inc.
- FDA Inspection 1315952 - 2026-04-30
- FDA Inspection 1215081 - 2023-08-17
- FDA Inspection 1032165 - 2017-11-17
- FDA Inspection 875205 - 2014-04-08
- FDA Inspection 740984 - 2011-08-19
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