FDA Inspection 1108510 — Robert Lehmann, Dr/Clin Inv

Robert Lehmann, Dr/Clin Inv — FEI 1000160285

The FDA completed an inspection of Robert Lehmann, Dr/Clin Inv on October 31, 2019 in Nacogdoches, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 31, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Nacogdoches, TX (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations