FDA Inspection 702339 — Catalina Offshore Products, Inc

Catalina Offshore Products, Inc — FEI 3000204855

The FDA completed an inspection of Catalina Offshore Products, Inc on Dec 15, 2010 in San Diego, CA. 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). 10 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 15, 2010
Fiscal Year
2011
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
San Diego, CA (United States)

Citations

IDCFRDescription
152421 CFR 123.11(b)Sanitation monitoring
600621 CFR 123.6(c)(7)Records values/observations
600821 CFR 123.8(a)(3)Verification - record review - frequency
601021 CFR 123.8(a)(3)(i)Monitoring record review adequacy
601821 CFR 123.7(a)Corrective action per predetermined plan
602021 CFR 123.9(a)Records - content
90521 CFR 123.6(b)HACCP plan implementation
93121 CFR 123.8(d)Verification - recordkeeping
94521 CFR 123.12(a)(2)Importer verification
96121 CFR 123.6(c)(3)Critical limits

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