FDA Inspection
Innovative Products Unlimited, IncInnovative Products Unlimited, Inc – FDA Inspection, May 16, 2017
Record Details
This FDA Inspection record concerns Innovative Products Unlimited, Inc, with an inspection on May 16, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Cynthia L. Aycock (Issuing Officer)
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ID · 06c2674e-49ac-4938-9946-e823578c6122
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1013081
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 820.198(d)Records of MDR Investigation
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.70(a)Production processes
- 21 CFR 820.180(b)Retention period
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Other FDA inspections of Innovative Products Unlimited, Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 16, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 15, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Innovative Products Unlimited, Inc
- FDA Inspection 783647 - 2012-05-16
- FDA Inspection 657664 - 2010-04-15
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