Hochland Deutschland GmbH, Schongau FDA Record

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

  • Latest inspection NAI · Jan 29, 2013
  • No warning letters matched by name
Inspections 1 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

Hochland Deutschland GmbH, Schongau has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Hochland Deutschland GmbH, Schongau" is on file.

What these totals cover: FDA records filed under the name "Hochland Deutschland GmbH, Schongau".

Latest inspection
Jan 29, 2013 · NAI

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
Inspections1Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Reviewing Hochland Deutschland GmbH, Schongau 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 Hochland Deutschland GmbH, Schongau 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

1 inspection on Jan 29, 2013.

DateSiteProductClassificationFEI
Jan 29, 2013Schongau, GermanyFood/CosmeticsNo Action Indicated (NAI)3004252048
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 3004252048Schongau, Germany1Jan 29, 2013

Hochland Deutschland GmbH, Schongau and the FDA: common questions

Has Hochland Deutschland GmbH, Schongau received an FDA warning letter?

No FDA warning letter addressed to the name "Hochland Deutschland GmbH, Schongau" 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 Hochland Deutschland GmbH, Schongau received an FDA Form 483?

FDA has not published a Form 483 for "Hochland Deutschland GmbH, Schongau" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Hochland Deutschland GmbH, Schongau?

The most recent FDA inspection on file ended Jan 29, 2013 at Schongau, Germany and was classified NAI. FDA has 1 inspection of Hochland Deutschland GmbH, Schongau on file.

Need more than this page shows? Ask about Hochland Deutschland GmbH, Schongau 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.