FDA Inspection 1074331 — DiversPack BV

DiversPack BV — FEI 3013632293

The FDA completed an inspection of DiversPack BV on Dec 13, 2018 in Woerden. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 13, 2018
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Woerden (Netherlands)

Citations

IDCFRDescription
1814721 CFR 117.35(e)Sanitation of non-food-contact surfaces - Manner and frequency

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.