FDA Inspection 1031756 — Kretek International, Inc.
The FDA completed an inspection of Kretek International, Inc. on November 7, 2017 in Moorpark, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Tobacco.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 7, 2017
- Fiscal Year
- 2018
- Product Type
- Tobacco
- Project Area
- Tobacco Post-Market Activities
- Location
- Moorpark, CA (United States)