# FDA Inspection 1278031 - SQ Products AG - August 07, 2025

Source: https://www.keypedia.com/records/fda_inspections/sq-products-ag/04310820-731f-425a-959e-1fad5b30e985
Source feed: FDA_Inspections

> FDA Inspection 1278031 for SQ Products AG on August 07, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1278031
- Company Name: SQ Products AG
- Inspection Date: 2025-08-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1278031 - 2025-08-07](https://www.keypedia.com/records/fda_inspections/sq-products-ag/542d2585-cd5e-4bac-8e98-da8d4a2275a2)
- [FDA Inspection 1065388 - 2018-07-05](https://www.keypedia.com/records/fda_inspections/sq-products-ag/59c23f98-adf7-49da-8ea5-73f3f58f0a4d)

Company: https://www.keypedia.com/companies/sq-products-ag/03dea5eb-cc42-4d2e-9efc-93446e921527

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