FDA Inspection 989559 — ALDI Inc.

ALDI Inc. — FEI 3007048809

The FDA completed an inspection of ALDI Inc. on Oct 20, 2016 in South Windsor, CT. 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). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 20, 2016
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
South Windsor, CT (United States)

Citations

IDCFRDescription
600421 CFR 123.6(c)(4)Monitoring - adequacy
601521 CFR 123.6(c)(6)Verification procedures - none/frequency
96321 CFR 123.6(c)(5)Corrective action plan

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.