FDA Inspection 1256884 — Mary Hughes, M.D.

Mary Hughes, M.D. — FEI 3032318917

The FDA completed an inspection of Mary Hughes, M.D. on Nov 21, 2024 in Greenville, SC. 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 21, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Greenville, SC (United States)

Additional Details

Clinical Investigator (CI)

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