FDA Inspection 1021721 — Kwekerij Mooijman BV
The FDA completed an inspection of Kwekerij Mooijman BV on May 9, 2017 in Nootdorp. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- May 9, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Nootdorp (Netherlands)