FDA Inspection
Medtox Diagnostics IncMedtox Diagnostics Inc – FDA Inspection, Dec 13, 2012
Record Details
This FDA Inspection record concerns Medtox Diagnostics Inc, with an inspection on December 13, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medtox Diagnostics Inc
- Inspection Date
- December 13, 2012
- Product Type
- Devices
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ID · addba4ad-424e-4473-bf2e-1d5e8f1124b3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 831744
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.50(b)Supplier notification of changes
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Medtox Diagnostics Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 10, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medtox Diagnostics Inc
- FDA Inspection 1007155 - 2017-02-10
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