FDA Inspection 1169754 — Robert L. Tychsen, MD

Robert L. Tychsen, MD — FEI 3021211428

The FDA completed an inspection of Robert L. Tychsen, MD on Mar 11, 2022 in Saint Louis, MO. 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 11, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)