FDA Inspection 1148056 — ActiveHerb Technology, Inc

ActiveHerb Technology, Inc — FEI 3006571191

The FDA completed an inspection of ActiveHerb Technology, Inc on August 6, 2021 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 6, 2021
Fiscal Year
2021
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
San Diego, CA (United States)

Citations

IDCFRDescription
1582921 CFR 111.70(b)(1)Specifications - component identity
1583021 CFR 111.70(b)(2)Specifications-component purity, strength, composition
1584021 CFR 111.70(e)Specifications - contamination limits
1586221 CFR 111.75(a)(2)Appropriate tests, examinations; certificate of analysis
1595821 CFR 111.113(a)(5)Quality control returned dietary supplement; material review, disposition
1599621 CFR 111.127(e)Quality control operations packaging, labeling; material review, disposition