FDA Inspection 1155095 — Edward T. Murphy, M.D.

Edward T. Murphy, M.D. — FEI 3017905883

The FDA completed an inspection of Edward T. Murphy, M.D. on October 14, 2021 in Grand Rapids, MI. 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
October 14, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Grand Rapids, MI (United States)

Additional Details

Clinical Investigator (CI)