FDA Inspection 1091378 — Neurogenesis, Inc

Neurogenesis, Inc — FEI 1643782

The FDA completed an inspection of Neurogenesis, Inc on May 31, 2019 in League City, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 31, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
League City, TX (United States)

Citations

IDCFRDescription
1564121 CFR 111.453Written procedures - holding
1579621 CFR 111.430(b)Records - packaging, labeling operations
1580921 CFR 111.570(b)(1)Written procedures - product complaint; review, investigate