# FDA Inspection 1096551 - IQ PRODUCTS B.V. - July 17, 2019

Source: https://www.keypedia.com/records/fda_inspections/iq-products-bv/32470abb-e967-483f-8b3a-b20bbdda079b
Source feed: FDA_Inspections

> FDA Inspection 1096551 for IQ PRODUCTS B.V. on July 17, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1096551
- Company Name: IQ PRODUCTS B.V.
- Inspection Date: 2019-07-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1196607 - 2023-02-01](https://www.keypedia.com/records/fda_inspections/iq-products-bv/bc84ff9a-97e2-4e3c-bb6f-1fde8218a843)
- [FDA Inspection 1096551 - 2019-07-17](https://www.keypedia.com/records/fda_inspections/iq-products-bv/cf6ed330-0d63-4eb0-8279-7eea57317451)

Company: https://www.keypedia.com/companies/iq-products-bv/2974a080-2c6f-4215-9925-b4323f25332b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7