FDA Inspection 1274020 — Mark P. Christiansen, M.D.

Mark P. Christiansen, M.D. — FEI 3009569111

The FDA completed an inspection of Mark P. Christiansen, M.D. on Jun 23, 2025 in Walnut Creek, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 23, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Walnut Creek, CA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450821 CFR 812.140(a)(4)Investigator record of protocol deviations inadequate
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.