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FDA Inspection 1035886 — Ronald Luff, MD

Ronald Luff, MD — FEI 3013863136

The FDA completed an inspection of Ronald Luff, MD on Dec 19, 2017 in Teterboro, NJ. 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
Dec 19, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Teterboro, NJ (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.