FDA Inspection 1100746 — Swissport U.S.A.

Swissport U.S.A. — FEI 3001604662

The FDA completed an inspection of Swissport U.S.A. on August 28, 2019 in Honolulu, HI. 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
August 28, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Technical Assistance: Food and Cosmetics
Location
Honolulu, HI (United States)