FDA Inspection
IQ PRODUCTS B.V.IQ PRODUCTS B.V. – FDA Inspection, Feb 1, 2023
Record Details
This FDA Inspection record concerns IQ PRODUCTS B.V., with an inspection on February 1, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · bc84ff9a-97e2-4e3c-bb6f-1fde8218a843
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1196607
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.72(a)Equipment control activity documentation
- 21 CFR 820.72(a)Equipment control activity documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of IQ PRODUCTS B.V.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 17, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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