FDA Inspection 1113352 — Biotek, Inc.

Biotek, Inc. — FEI 3001236658

The FDA completed an inspection of Biotek, Inc. on December 20, 2019 in Layton, UT. 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
December 20, 2019
Fiscal Year
2020
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Layton, UT (United States)

Citations

IDCFRDescription
1594021 CFR 111.105(h)Quality control - production, process control