FDA Inspection 1043736 — John Meyer, MD

John Meyer, MD — FEI 3014209551

The FDA completed an inspection of John Meyer, MD on March 5, 2018 in Louisville, KY. 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
March 5, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Louisville, KY (United States)

Additional Details

Clinical Investigator (CI)