FDA Inspection 1025219 — 209 Port Of Almota
The FDA completed an inspection of 209 Port Of Almota on August 18, 2017 in Colfax, WA. 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 18, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Colfax, WA (United States)