FDA Inspection 1114129 — Lawrence Groop, DMD

Lawrence Groop, DMD — FEI 3015881076

The FDA completed an inspection of Lawrence Groop, DMD on December 20, 2019 in Scottsdale, AZ. 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
December 20, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Scottsdale, AZ (United States)

Additional Details

Clinical Investigator (CI)