FDA Inspection 1087456 — Pixotine Products, Inc.

Pixotine Products, Inc. — FEI 3013349494

The FDA completed an inspection of Pixotine Products, Inc. on Jan 15, 2019 in Jupiter, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Tobacco.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
Jan 15, 2019
Fiscal Year
2019
Product Type
Tobacco
Project Area
Tobacco Post-Market Activities
Location
Jupiter, FL (United States)