FDA Inspection 1301494 — Roquette America, Inc.

Roquette America, Inc. — FEI 1910565

The FDA completed an inspection of Roquette America, Inc. on January 30, 2026 in Keokuk, IA. 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
Keokuk, IA (United States)