FDA Inspection 749625 — Fitrite Incorporated

Fitrite Incorporated — FEI 3004262563

The FDA completed an inspection of Fitrite Incorporated on April 29, 2011 in Quezon City. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 7 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 29, 2011
Fiscal Year
2011
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Quezon City (Philippines)

Citations

IDCFRDescription
104021 CFR 113.10Operators
125821 CFR 113.60(c)Coding - visible
131621 CFR 113.87(c)Initial temperature of container contents
152921 CFR 113.89Process deviation log/file
173421 CFR 113.40(a)(2)(iii)Adjusted to agree with TID
210121 CFR 113.40(a)(13)Measured, recorded
387421 CFR 113.60(b)Cooling water - not chlorinated, sanitized