Heiden's Inc FDA Inspection Record

FEI 2010832 · Inspections, Form 483s, warning letters and import refusals

Heiden's Inc is an FDA-inspected facility (FEI 2010832) located in Anaheim, CA, US. RegDataLab tracks 5 FDA inspections at this facility.

Reviewing Heiden's Inc as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Heiden's Inc yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

What FDA found at this site

Latest inspection
Apr 29, 2025: No Action Indicated (NAI)
Inspections on record
5 (2 VAI, 3 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
Apr 29, 2025No Action Indicated (NAI)No citations listed
Aug 8, 2017No Action Indicated (NAI)No citations listed
May 12, 2014Voluntary Action Indicated (VAI)Precluding contaminants (21 CFR 110.40(a))
Mar 3, 2011Voluntary Action Indicated (VAI)Food-contact - corrosion resistant (21 CFR 110.40(a))
Storage requirements (21 CFR 110.35(b)(2))
Maintenance of processing and production records (21 CFR 114.100(b))
Mar 2, 2010No Action Indicated (NAI)No citations listed

Facility details

Company
Heiden's Inc
Location
Anaheim, CA (US)
Source
inspections

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