FDA Inspection 1121898 — Loyd S. Godwin, M.D.

Loyd S. Godwin, M.D. — FEI 3016270815

The FDA completed an inspection of Loyd S. Godwin, M.D. on March 10, 2020 in Shelton, CT. 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 10, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Shelton, CT (United States)

Additional Details

Clinical Investigator (CI)