Home / Companies / Arevipharma GmbH

Arevipharma GmbH

FDA Regulatory Profile

Arevipharma GmbH has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 20, 2025 · VAI

Reviewing Arevipharma GmbH 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 Arevipharma GmbH 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

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections5Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 20, 2025Radebeul, GermanyDrugsVoluntary Action Indicated (VAI)1000505976
Sep 16, 2019Radebeul, GermanyDrugsNo Action Indicated (NAI)1000505976
Apr 29, 2016Radebeul, GermanyDrugsNo Action Indicated (NAI)1000505976
Nov 16, 2012Radebeul, GermanyDrugsNo Action Indicated (NAI)1000505976
Apr 8, 2009Radebeul, GermanyVeterinaryVoluntary Action Indicated (VAI)1000505976

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 1000505976Radebeul, Germany5Jun 20, 2025

FDA data resources

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