New Kam Man LLC FDA Inspection Record

FEI 3004259846 · Inspections, Form 483s, warning letters and import refusals

New Kam Man LLC is an FDA-inspected facility (FEI 3004259846) located in New York, NY, US. RegDataLab tracks 3 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
May 1, 2025: Voluntary Action Indicated (VAI)
Inspections on record
3 (3 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
May 1, 2025Voluntary Action Indicated (VAI)Develop FSVP (21 CFR 1.502(a))
Mar 16, 2020Voluntary Action Indicated (VAI)Sanitary operations - Plant maintenance (21 CFR 117.35(a))
Manufacturing, processing, packing, holding - Controls (21 CFR 117.80(c))
Apr 4, 2019Voluntary Action Indicated (VAI)Sanitary operations - Plant maintenance (21 CFR 117.35(a))
Pest control (21 CFR 117.35(c))
Manufacturing, processing, packing, holding - Controls (21 CFR 117.80(c))

Facility details

Company
New Kam Man LLC
Location
New York, NY (US)
Source
inspections

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