FDA Inspection 1034795 — UNIFI

UNIFI — FEI 3004401346

The FDA completed an inspection of UNIFI on Nov 16, 2017 in Portland, ME. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 16, 2017
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Technical Assistance: Food and Cosmetics
Location
Portland, ME (United States)

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