FDA Inspection
IQ PRODUCTS B.V.IQ PRODUCTS B.V. – FDA Inspection, Jul 17, 2019
Record Details
This FDA Inspection record concerns IQ PRODUCTS B.V., with an inspection on July 17, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · cf6ed330-0d63-4eb0-8279-7eea57317451
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1096551
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.20(a)Quality policy and objectives
- 21 CFR 820.50(b)Supplier notification of changes
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Other FDA inspections of IQ PRODUCTS B.V.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 1, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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