FDA Inspection 910003 — Unifi

Unifi — FEI 3005658288

The FDA completed an inspection of Unifi on Jan 16, 2015 in Cheektowaga, NY. 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). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 16, 2015
Fiscal Year
2015
Product Type
Food/Cosmetics
Project Area
Technical Assistance: Food and Cosmetics
Location
Cheektowaga, NY (United States)

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