FDA Inspection 1013563 — Altiza Inc.

Altiza Inc. — FEI 3006329724

The FDA completed an inspection of Altiza Inc. on May 1, 2017 in Chula Vista, 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
May 1, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Chula Vista, CA (United States)

Citations

IDCFRDescription
142721 CFR 110.20(b)(5)Safety lighting and glass