FDA Inspection 1010506 — Merion Inc.

Merion Inc. — FEI 2000046171

The FDA completed an inspection of Merion Inc. on February 9, 2017 in West Covina, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 9, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
West Covina, CA (United States)

Citations

IDCFRDescription
1564121 CFR 111.453Written procedures - holding
1583921 CFR 111.70(e)Specifications - identity, purity, strength, composition
1585321 CFR 111.73Specifications met - identity, purity, strength, composition
1592721 CFR 111.103Written procedures - quality control operations
1593221 CFR 111.105(a)Quality control - processes, specifications, written procedures