# FDA Inspection 1279413 - Sanguina, Inc. - August 20, 2025

Source: https://www.keypedia.com/records/fda_inspections/sanguina-inc/3e360daf-ed10-456c-944a-5ab4531ad2c6
Source feed: FDA_Inspections

> FDA Inspection 1279413 for Sanguina, Inc. on August 20, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1279413
- Company Name: Sanguina, Inc.
- Inspection Date: 2025-08-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1279413 - 2025-08-20](https://www.keypedia.com/records/fda_inspections/sanguina-inc/6fc86703-8c3a-4f6b-8db9-b1b7662c1e08)
- [FDA Inspection 1279413 - 2025-08-20](https://www.keypedia.com/records/fda_inspections/sanguina-inc/6f4c7729-1778-451a-994b-67b19007ae35)

Company: https://www.keypedia.com/companies/sanguina-inc/21fe47df-7481-4b36-a936-181d6e6c4f78

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