FDA Inspection 1247930 — Susan Seedman, M.D.

Susan Seedman, M.D. — FEI 3031510850

The FDA completed an inspection of Susan Seedman, M.D. on Aug 30, 2024 in Rio Rancho, NM. 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
Aug 30, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Rio Rancho, NM (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
765921 CFR 50.25(a)(6)Compensation, medical treatment in event of injury