FDA Inspection 1102109 — Kretek International, Inc.
The FDA completed an inspection of Kretek International, Inc. on July 31, 2019 in Moorpark, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Tobacco.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 31, 2019
- Fiscal Year
- 2019
- Product Type
- Tobacco
- Project Area
- Tobacco Post-Market Activities
- Location
- Moorpark, CA (United States)