FDA Inspection 1300634 — FISHFA BIOGENICS

FISHFA BIOGENICS — FEI 3017150186

The FDA completed an inspection of FISHFA BIOGENICS on January 30, 2026 in Rajkot. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 30, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rajkot (India)