FDA Inspection
VicTorch Meditek, IncVicTorch Meditek, Inc – FDA Inspection, Sep 15, 2014
Record Details
This FDA Inspection record concerns VicTorch Meditek, Inc, with an inspection on September 15, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- VicTorch Meditek, Inc
- Inspection Date
- September 15, 2014
- Product Type
- Devices
View Company Profile
ID · 6f33fd8c-e80e-478f-a3de-3bb63963ce62
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 895393
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.30(a)Design control - no procedures
- 21 CFR 820.250(b)Sampling plans
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Other FDA inspections of VicTorch Meditek, Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| October 18, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 17, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 19, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for VicTorch Meditek, Inc
- FDA Inspection 1106828 - 2019-10-18
- FDA Inspection 1066293 - 2018-09-17
- FDA Inspection 775766 - 2012-03-19
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