FDA Inspection
Preventive Technologies IncPreventive Technologies Inc – FDA Inspection, Apr 19, 2018
Record Details
This FDA Inspection record concerns Preventive Technologies Inc, with an inspection on April 19, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 7df53870-c007-46d1-8b45-3c126fc61a06
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1049219
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Preventive Technologies Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 21, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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