HEARTLAND SOCIETY OF NORTHERN CA INC. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

  • Latest inspection VAI · Sep 28, 2022
  • No warning letters matched by name
Inspections 3 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

HEARTLAND SOCIETY OF NORTHERN CA INC. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "HEARTLAND SOCIETY OF NORTHERN CA INC." is on file.

What these totals cover: FDA records filed under the name "HEARTLAND SOCIETY OF NORTHERN CA INC." and its spelling variant "Heartland Society Of Northern Ca".

Latest inspection
Sep 28, 2022 · VAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 11, 2026 (checked Nov 15, 2026, unchanged)File dated Nov 10, 2026Current
510(k) clearances0Nov 15, 2026File dated Nov 9, 2026Current
Inspections3Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

HEARTLAND SOCIETY OF NORTHERN CA INC.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

HEARTLAND SOCIETY OF NORTHERN CA INC.: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202300000
202210000
202110000
202000000
201900000
201810000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Reviewing HEARTLAND SOCIETY OF NORTHERN CA 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 HEARTLAND SOCIETY OF NORTHERN CA 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

Recent FDA inspections

3 inspections from Sep 19, 2018 to Sep 28, 2022.

DateSiteProductClassificationFEI
Sep 28, 2022San Jose, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013159991
Aug 9, 2021San Jose, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013159991
Sep 19, 2018San Jose, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013159991
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3013159991San Jose, CA3Sep 28, 2022

HEARTLAND SOCIETY OF NORTHERN CA INC. and the FDA: common questions

Has HEARTLAND SOCIETY OF NORTHERN CA INC. received an FDA warning letter?

No FDA warning letter addressed to the name "HEARTLAND SOCIETY OF NORTHERN CA INC." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has HEARTLAND SOCIETY OF NORTHERN CA INC. received an FDA Form 483?

FDA has not published a Form 483 for "HEARTLAND SOCIETY OF NORTHERN CA INC." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect HEARTLAND SOCIETY OF NORTHERN CA INC.?

The most recent FDA inspection on file ended Sep 28, 2022 at San Jose, CA and was classified VAI. FDA has 3 inspections of HEARTLAND SOCIETY OF NORTHERN CA INC. on file.

Need more than this page shows? Ask about HEARTLAND SOCIETY OF NORTHERN CA INC. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

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