# FDA Inspection 1251706 - Veridiam, Inc. - October 10, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/veridiam-inc/ff6e384e-a5d4-4147-8611-99070d0d4c92/
Source feed: FDA_Inspections

> FDA Inspection 1251706 for Veridiam, Inc. on October 10, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1251706
- Company Name: Veridiam, Inc.
- Inspection Date: 2024-10-10
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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Company: https://www.globalkeysolutions.net/companies/veridiam-inc/212aead5-2add-404e-af37-581884cf8f29

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