FDA Inspection 1067099 — Reverb Coffee Company

Reverb Coffee Company — FEI 3010908504

The FDA completed an inspection of Reverb Coffee Company on Aug 30, 2018 in Memphis, TN. 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
Aug 30, 2018
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Memphis, TN (United States)