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FDA Inspection 1080585 — Yannis Raftopoulos, MD

Yannis Raftopoulos, MD — FEI 3014768452

The FDA completed an inspection of Yannis Raftopoulos, MD on Feb 7, 2019 in Holyoke, MA. 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 7, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Holyoke, MA (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.