FDA Inspection 803278 — Gulfish L.P.

Gulfish L.P. — FEI 3009222439

The FDA completed an inspection of Gulfish L.P. on October 19, 2012 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). 4 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 19, 2012
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
San Francisco, CA (United States)

Citations

IDCFRDescription
601621 CFR 123.6(c)(7)Records system
601721 CFR 123.7(c)Corrective action per regulation
90821 CFR 123.6(d)Signed and dated
96321 CFR 123.6(c)(5)Corrective action plan