FDA Inspection 683134 — Max V. McLaughlin, M.D.

Max V. McLaughlin, M.D. — FEI 3008420919

The FDA completed an inspection of Max V. McLaughlin, M.D. on Sep 16, 2010 in Mobile, AL. 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
Sep 16, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Mobile, AL (United States)

Additional Details

Clinical Investigator (CI)