Plantin America, Inc. FDA Inspection Record

FEI 3011365703 · Inspections, Form 483s, warning letters and import refusals

Plantin America, Inc. is an FDA-inspected facility (FEI 3011365703) located in New York, NY, US. RegDataLab tracks 5 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Dec 9, 2025: No Action Indicated (NAI)
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
Dec 9, 2025No Action Indicated (NAI)No citations listed
Jul 21, 2022Voluntary Action Indicated (VAI)Develop FSVP (21 CFR 1.502(a))
Hazard analysis biological, chemical, physical (21 CFR 1.504(b)(1))
Evaluation - performance, risk (21 CFR 1.505(a)(2))
Supplier verification - establish written procedures (21 CFR 1.506(b))
and 1 more
Feb 19, 2020Voluntary Action Indicated (VAI)Develop FSVP (21 CFR 1.502(a))
Jul 30, 2018Voluntary Action Indicated (VAI)No citations listed
Oct 30, 2015No Action Indicated (NAI)No citations listed

Facility details

Company
Plantin America, Inc.
Location
New York, NY (US)
Source
inspections

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