FDA Inspection 808589 — PureTek Corporation
The FDA completed an inspection of PureTek Corporation on December 4, 2012 in San Fernando, CA. 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
- December 4, 2012
- Fiscal Year
- 2013
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- San Fernando, CA (United States)