FDA Inspection 781691 — Unifi

Unifi — FEI 1000306773

The FDA completed an inspection of Unifi on May 9, 2012 in Rapid City, SD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 9, 2012
Fiscal Year
2012
Product Type
Food/Cosmetics
Project Area
Technical Assistance: Food and Cosmetics
Location
Rapid City, SD (United States)