FDA Inspection 861173 — Cayenne Company, Inc

Cayenne Company, Inc — FEI 1000116258

The FDA completed an inspection of Cayenne Company, Inc on Dec 23, 2013 in Andover, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 15 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 23, 2013
Fiscal Year
2014
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Andover, MN (United States)

Citations

IDCFRDescription
1538121 CFR 111.8Written procedures - hygienic practices
1545321 CFR 111.16Written procedures - cleaning
1549121 CFR 111.25Equipment - procedures
1553221 CFR 111.255(b)Batch record - complete
1557021 CFR 111.153Written procedures - components
1561921 CFR 111.180(b)(1)Written procedures - packaging, labeling received
1564121 CFR 111.453Written procedures - holding
1576221 CFR 111.205(a)Master manufacturing record - each batch
1579721 CFR 111.553Written procedures - product complaint
1583921 CFR 111.70(e)Specifications - identity, purity, strength, composition
1585821 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
1586121 CFR 111.75(a)(2)(ii)(A)Component - qualify supplier
1589721 CFR 111.83(a)Reserve sample - collect, hold
1592721 CFR 111.103Written procedures - quality control operations
1604221 CFR 111.503Written procedures - returned dietary supplement