FDA Inspection 1202009 — Glynis Ablon, M.D.

Glynis Ablon, M.D. — FEI 3012330175

The FDA completed an inspection of Glynis Ablon, M.D. on March 24, 2023 in Manhattan Beach, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 24, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Manhattan Beach, CA (United States)

Additional Details

Clinical Investigator (CI)