# FDA Inspection 1274020 - Mark P. Christiansen, M.D. - June 23, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/mark-p-christiansen-md/81283ed4-8122-4a4e-8ea7-a53a9d2a57da
Source feed: FDA_Inspections

> FDA Inspection 1274020 for Mark P. Christiansen, M.D. on June 23, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1274020
- Company Name: Mark P. Christiansen, M.D.
- Inspection Date: 2025-06-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1274020 - 2025-06-23](https://www.globalkeysolutions.net/records/fda_inspections/mark-p-christiansen-md/c8ce0fbb-564e-45b9-b5a7-b3a2051960eb)
- [FDA Inspection 1080168 - 2019-02-12](https://www.globalkeysolutions.net/records/fda_inspections/mark-p-christiansen-md/9067db03-0c8d-48ab-8799-c1c0b4bfdb0a)
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Company: https://www.globalkeysolutions.net/companies/mark-p-christiansen-md/bf635817-3dfc-46fd-84c4-3b014edd93d6

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