FDA Inspection 760049 — ORBE, S.A.

ORBE, S.A. — FEI 3013022970

The FDA completed an inspection of ORBE, S.A. on Dec 16, 2011 in Vigo. 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). 4 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 16, 2011
Fiscal Year
2012
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Vigo (Spain)

Citations

IDCFRDescription
133121 CFR 113.100(a)(1)Still retorts
210121 CFR 113.40(a)(13)Measured, recorded
385921 CFR 113.60(a)Frequency: visual closure examinations, record
387721 CFR 113.60(c)Coding - required elements

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