FDA Inspection 987041 — Lyoferm, Inc.

Lyoferm, Inc. — FEI 3010082322

The FDA completed an inspection of Lyoferm, Inc. on August 24, 2016 in Greenfield, IN. 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
August 24, 2016
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Greenfield, IN (United States)