FDA Inspection 1206677 — Veloxis Pharmaceuticals, Inc.

Veloxis Pharmaceuticals, Inc. — FEI 3008678603

The FDA completed an inspection of Veloxis Pharmaceuticals, Inc. on May 19, 2023 in Cary, NC. 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
May 19, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cary, NC (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)