FDA Inspection 1014525 — Charles Lambert, M.D.

Charles Lambert, M.D. — FEI 3013130365

The FDA completed an inspection of Charles Lambert, M.D. on June 5, 2017 in Tampa, FL. 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
June 5, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tampa, FL (United States)

Additional Details

Clinical Investigator (CI)