# FDA Inspection 1251722 - Dignitana, Inc. - November 05, 2024

Source: https://www.keypedia.com/records/fda_inspections/dignitana-inc/01a45e0a-11ab-4e58-a0f7-738ceebb54b0
Source feed: FDA_Inspections

> FDA Inspection 1251722 for Dignitana, Inc. on November 05, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1251722
- Company Name: Dignitana, Inc.
- Inspection Date: 2024-11-05
- 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 1251722 - 2024-11-05](https://www.keypedia.com/records/fda_inspections/dignitana-inc/0f26bd83-fb11-4c92-b052-e26f133afb73)
- [FDA Inspection 1251722 - 2024-11-05](https://www.keypedia.com/records/fda_inspections/dignitana-inc/d571bc00-4766-44f0-8f95-c91d492728c6)
- [FDA Inspection 1251722 - 2024-11-05](https://www.keypedia.com/records/fda_inspections/dignitana-inc/5eaf7c36-d239-4cd5-afb9-425600c23182)

Company: https://www.keypedia.com/companies/dignitana-inc/71aad248-c02a-4750-b151-a2a1e33198fe

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