FDA Inspection 791806 — Anafit, Inc.

Anafit, Inc. — FEI 3009669917

The FDA completed an inspection of Anafit, Inc. on August 7, 2012 in Orlando, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 7 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 7, 2012
Fiscal Year
2012
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Orlando, FL (United States)

Citations

IDCFRDescription
1564121 CFR 111.453Written procedures - holding
1576221 CFR 111.205(a)Master manufacturing record - each batch
1579621 CFR 111.430(b)Records - packaging, labeling operations
1579721 CFR 111.553Written procedures - product complaint
1582821 CFR 111.70(a)Specifications - manufacturing process
1592821 CFR 111.103Written procedure quality control operations material review
1604221 CFR 111.503Written procedures - returned dietary supplement