FDA Inspection 973802 — Lawrence B Katzen, DVM

Lawrence B Katzen, DVM — FEI 3005942826

The FDA completed an inspection of Lawrence B Katzen, DVM on May 12, 2016 in Boynton Beach, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 12, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Boynton Beach, FL (United States)

Additional Details

Clinical Investigator (CI)