FDA Inspection 971438 — Robert Lehmann, Dr/Clin Inv

Robert Lehmann, Dr/Clin Inv — FEI 1000160285

The FDA completed an inspection of Robert Lehmann, Dr/Clin Inv on May 5, 2016 in Nacogdoches, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 5, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Nacogdoches, TX (United States)

Additional Details

Clinical Investigator (CI)