FDA Inspection 1144663 — Roquette America, Inc.

Roquette America, Inc. — FEI 1910565

The FDA completed an inspection of Roquette America, Inc. on June 17, 2021 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
June 17, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Keokuk, IA (United States)