FDA Inspection 1249655 — Keith A. Marcus, M.D.

Keith A. Marcus, M.D. — FEI 3031260195

The FDA completed an inspection of Keith A. Marcus, M.D. on September 12, 2024 in Redondo Beach, CA. 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
September 12, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Redondo Beach, CA (United States)

Additional Details

Clinical Investigator (CI)