FDA Inspection 983351 — Roquette America, Inc.
The FDA completed an inspection of Roquette America, Inc. on August 3, 2016 in Keokuk, IA. 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
- August 3, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Keokuk, IA (United States)