FDA Inspection 1001307 — Thomas Haldis, M.D.

Thomas Haldis, M.D. — FEI 3013040547

The FDA completed an inspection of Thomas Haldis, M.D. on Feb 14, 2017 in Fargo, ND. 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 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Fargo, ND (United States)

Additional Details

Clinical Investigator (CI)

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