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HEB FDA Inspection Record

FEI 3016789985 · Inspections, Form 483s, warning letters and import refusals

HEB (FEI 3016789985) located in San Antonio, TX, United States has FDA compliance records.

What FDA found at this site

Inspections on record
None in FDA's published inspection data
Warning letters
1 listed by FDA for this FEI, latest Sep 23, 2021

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.

FDA record score

Not scored. FDA's published inspection data has no inspection for this site, and the score is only counted for inspected sites. This is not a score of 0. The records FDA does list for this FEI are below.

Counted on Nov 14, 2026, method version 1. How this is counted.

1 record FDA lists for this FEI
RecordDatePoints x age weightAdds
Warning letter on FDA's dashboard, which does not show close-outsSep 23, 2021The site is not scored, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Location
San Antonio, TX (United States)

Compliance actions

FDA data resources

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