FDA Inspection 1074172 — Barnthouse, Dr Joseph

Barnthouse, Dr Joseph — FEI 3005691380

The FDA completed an inspection of Barnthouse, Dr Joseph on Nov 15, 2018 in Kansas City, MO. 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
Nov 15, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Kansas City, MO (United States)

Additional Details

Clinical Investigator (CI)