FDA Inspection
Mark P. Christiansen, M.D.Mark P. Christiansen, M.D. – FDA Inspection, Jun 23, 2025
Record Details
This FDA Inspection record concerns Mark P. Christiansen, M.D., with an inspection on June 23, 2025, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- Mark P. Christiansen, M.D.
- Inspection Date
- June 23, 2025
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · c8ce0fbb-564e-45b9-b5a7-b3a2051960eb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1274020
- FDA center
- Medical Devices & Rad Health
- Project area
- Product Evaluation: Medical Devices
FDA Citations
2- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(4)Investigator record of protocol deviations inadequate
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Mark P. Christiansen, M.D.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 12, 2019 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| March 9, 2017 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 30, 2014 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| July 12, 2012 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Mark P. Christiansen, M.D.
- FDA Inspection 1080168 - 2019-02-12
- FDA Inspection 1015109 - 2017-03-09
- FDA Inspection 906161 - 2014-10-30
- FDA Inspection 791814 - 2012-07-12
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