FDA Inspection
Medical Technology ProductsMedical Technology Products – FDA Inspection, Jan 12, 2010
Record Details
This FDA Inspection record concerns Medical Technology Products, with an inspection on January 12, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medical Technology Products
- Inspection Date
- January 12, 2010
- Product Type
- Devices
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ID · d26d256b-7ab0-4f70-a2f8-f638a72610ee
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 638786
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)General
- 21 CFR 820.22Quality Audit/Reaudit - conducted
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Other FDA inspections of Medical Technology Products
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 1, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 1, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 17, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medical Technology Products
- FDA Inspection 1150920 - 2021-09-01
- FDA Inspection 928855 - 2015-05-01
- FDA Inspection 791452 - 2012-07-17
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