FDA Inspection 1098684 — Thomas Lavin, MD

Thomas Lavin, MD — FEI 3015403145

The FDA completed an inspection of Thomas Lavin, MD on July 22, 2019 in Metairie, LA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 22, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Metairie, LA (United States)

Additional Details

Clinical Investigator (CI)