FDA Inspection 991993 — Kretek International, Inc.
The FDA completed an inspection of Kretek International, Inc. on October 27, 2016 in Moorpark, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Tobacco.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- October 27, 2016
- Fiscal Year
- 2017
- Product Type
- Tobacco
- Project Area
- Tobacco Post-Market Activities
- Location
- Moorpark, CA (United States)