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FDA Inspection 1073424 — Miller, Hugh MD

Miller, Hugh MD — FEI 3002741750

The FDA completed an inspection of Miller, Hugh MD on Nov 1, 2018 in Tucson, AZ. 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 1, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tucson, AZ (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources