FDA Inspection 1091956 — Neurogan, Inc.

Neurogan, Inc. — FEI 3014305326

The FDA completed an inspection of Neurogan, Inc. on June 5, 2019 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 5, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
San Diego, CA (United States)

Additional Details

FSVP

Citations

IDCFRDescription
1825421 CFR 1.502(a)Develop FSVP