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Intercibus, Inc. — FDA Facility Profile

FEI 3004344619

Intercibus, Inc. is an FDA-inspected facility (FEI 3004344619) located in Brookside, NJ, US. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
Mar 23, 2021: Voluntary Action Indicated (VAI)
Inspections on record
1 (1 VAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Mar 23, 2021Voluntary Action Indicated (VAI)Hazard analysis biological, chemical, physical (21 CFR 1.504(b)(1))
Record - translate to English (21 CFR 1.510(b)(1))

Facility details

Company
Intercibus, Inc.
Location
Brookside, NJ (US)
Source
inspections

FDA data resources

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