FDA Inspection 1201351 — Melanie Palm, MD

Melanie Palm, MD — FEI 3021245717

The FDA completed an inspection of Melanie Palm, MD on February 23, 2023 in Solana 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
February 23, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Solana Beach, CA (United States)

Additional Details

Clinical Investigator (CI)