FDA Inspection 1032307 — Neviot Corp.

Neviot Corp. — FEI 3004279624

The FDA completed an inspection of Neviot Corp. on November 27, 2017 in Arverne, NY. 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
November 27, 2017
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Arverne, NY (United States)