FDA Inspection 1084156 — Jerome M. Wiater, M.D.

Jerome M. Wiater, M.D. — FEI 3014672595

The FDA completed an inspection of Jerome M. Wiater, M.D. on Feb 25, 2019 in Royal Oak, MI. 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
Feb 25, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Royal Oak, MI (United States)

Additional Details

Clinical Investigator (CI)

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