# FDA Inspection 1221106 - Valensil - October 12, 2023

Source: https://www.keypedia.com/records/fda_inspections/valensil/141b87cf-7587-4e44-b8c8-be8f9a89c61b
Source feed: FDA_Inspections

> FDA Inspection 1221106 for Valensil on October 12, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1221106
- Company Name: Valensil
- Inspection Date: 2023-10-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1221106 - 2023-10-12](https://www.keypedia.com/records/fda_inspections/valensil/46165379-6d0b-4702-89db-3c3bb5cb72d7)

Company: https://www.keypedia.com/companies/valensil/adb3a1d5-6232-4e27-8e1d-03d9652525be

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