FDA Inspection
Preventive Technologies IncPreventive Technologies Inc – FDA Inspection, Nov 21, 2014
Record Details
This FDA Inspection record concerns Preventive Technologies Inc, with an inspection on November 21, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Preventive Technologies Inc
- Inspection Date
- November 21, 2014
- Product Type
- Devices
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ID · d556caa3-c584-4852-85ee-2e907f5da5a1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 905565
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.50(b)Supplier notification of changes
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Other FDA inspections of Preventive Technologies Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 19, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Preventive Technologies Inc
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