FDA Inspection 944095 — Fitrite Incorporated

Fitrite Incorporated — FEI 3004262563

The FDA completed an inspection of Fitrite Incorporated on Sep 1, 2015 in Quezon City. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 7 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 1, 2015
Fiscal Year
2015
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Quezon City (Philippines)

Citations

IDCFRDescription
128721 CFR 110.20(a)(1)Harborage areas
129221 CFR 110.20(b)(1)Sufficient space
130621 CFR 110.20(b)(7)Screening
156021 CFR 110.35(c)Lack of effective pest exclusion
159721 CFR 110.37(b)(3)As source of contamination
169821 CFR 110.80(b)(5)Work-in-progress
307121 CFR 114.80(a)(1)Scheduled process

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.