# Mark P. Christiansen, M.D. – FDA Inspection, Jun 23, 2025

Source: https://www.keypedia.com/records/fda_inspections/mark-p-christiansen-md/c8ce0fbb-564e-45b9-b5a7-b3a2051960eb
Source feed: FDA_Inspections

> FDA inspection 1274020 of Mark P. Christiansen, M.D., June 23, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 4 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: San Francisco District Office
- Citation Count: 2

## Related Documents

- FDA Inspection 1080168 - 2019-02-12
- [FDA Inspection 1015109 - 2017-03-09](https://www.keypedia.com/records/fda_inspections/mark-p-christiansen-md/ca4542ce-bf8b-4f07-a8fa-21bcf1b885ed)
- FDA Inspection 906161 - 2014-10-30
- [FDA Inspection 791814 - 2012-07-12](https://www.keypedia.com/records/fda_inspections/mark-p-christiansen-md/b3d16109-cf42-45e3-a51d-d13a3800ab74)

## Related Officers

- [Investigator](https://www.keypedia.com/people/cynthia-j-tsui/e02b5fd2-e90b-47a7-bbc2-e658f160c4ae)

Company: https://www.keypedia.com/companies/mark-p-christiansen-md/bf635817-3dfc-46fd-84c4-3b014edd93d6

Office: https://www.keypedia.com/offices/san-francisco-district-office/6f838e9c-aae1-4665-9c46-a51d43be02df