FDA Inspection 1155900 — Eidon Inc.

Eidon Inc. — FEI 3004402329

The FDA completed an inspection of Eidon Inc. on November 3, 2021 in Poway, 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
November 3, 2021
Fiscal Year
2022
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Poway, CA (United States)

Citations

IDCFRDescription
1580221 CFR 111.560(c)Product complaint - review, investigation
1583921 CFR 111.70(e)Specifications - identity, purity, strength, composition
1584021 CFR 111.70(e)Specifications - contamination limits
1586221 CFR 111.75(a)(2)Appropriate tests, examinations; certificate of analysis
1595321 CFR 111.113(a)(1)Quality control production, process control; material review, disposition