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JAK Diversified II, Inc. Dba Multi-Pak Packaging — FDA Facility Profile

FEI 3003333011

JAK Diversified II, Inc. Dba Multi-Pak Packaging is an FDA-registered facility (FEI 3003333011) located in West Caldwell, NJ, US. Registered operations: LABEL; PACK; RELABEL; REPACK. RegDataLab tracks 5 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
May 1, 2024: Voluntary Action Indicated (VAI)
Inspections on record
5 (3 VAI, 2 NAI)
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
May 1, 2024Voluntary Action Indicated (VAI)Approve or reject components, products (21 CFR 211.22(a))
Cleaning / Sanitizing / Maintenance (21 CFR 211.67(a))
Absence of Written Procedures (21 CFR 211.100(a))
Dec 6, 2019Voluntary Action Indicated (VAI)Cleaning / Sanitizing / Maintenance (21 CFR 211.67(a))
Apr 29, 2016No Action Indicated (NAI)No citations listed
Jul 22, 2013No Action Indicated (NAI)No citations listed
Jan 31, 2011Voluntary Action Indicated (VAI)GMP Training Frequency (21 CFR 211.25(a))
Written procedures not established/followed (21 CFR 211.67(b))
Absence of Written Procedures (21 CFR 211.100(a))
Reprocessing procedures not written or followed (21 CFR 211.115(a))
and 2 more

Facility details

Company
JAK Diversified II Inc.
Location
West Caldwell, NJ (US)
Registration Expires
Dec 31, 2026
Operations
LABEL; PACK; RELABEL; REPACK
Source
both

FDA data resources

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