FDA Inspection 1004067 — Gulfish L.P.

Gulfish L.P. — FEI 3009222439

The FDA completed an inspection of Gulfish L.P. on February 15, 2017 in San Francisco, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 15, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
San Francisco, CA (United States)

Citations

IDCFRDescription
365221 CFR 110.37(e)(1)Suitable locations
93121 CFR 123.8(d)Verification - recordkeeping
93321 CFR 123.8(a)(2)(ii)Calibration - adequacy