# Arevipharma GmbH, Radebeul, Germany – FDA Inspections

Source: https://www.keypedia.com/companies/arevipharma-gmbh/d2cf1bd6-f918-449d-83e7-70065b9cb728

> Inspection records and compliance data for Arevipharma GmbH in Radebeul. 5 FDA inspections on record, last inspected June 20, 2025.

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## Details

- Name: Arevipharma GmbH
- FEI Number: 1000505976
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING
- Address Line 1: Meisner Str. 35
- City: Radebeul
- Country Name: Germany
- Address: Meisner Str. 35, Radebeul, Germany
- Country: Germany

## Related Documents

- [FDA Inspection 1288700 - Arevipharma GmbH - 2025-06-20](https://www.keypedia.com/records/fda_inspections/arevipharma-gmbh/c286f0d5-f5e5-4af8-b1d5-56d82a663486) — source: FDA, date: June 20, 2025
- FDA Inspection 1288700 - Arevipharma GmbH - 2025-06-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 20, 2025
- [FDA Inspection 1141793 - Arevipharma GmbH - 2019-09-16](https://www.keypedia.com/records/fda_inspections/arevipharma-gmbh/d795ea7c-d802-42db-ae9e-0fbc04a1d9ab) — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2019
- FDA Inspection 969875 - Arevipharma GmbH - 2016-04-29 — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2016
- FDA Inspection 808573 - Arevipharma GmbH - 2012-11-16 — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2012
- FDA Inspection 576014 - Arevipharma GmbH - 2009-04-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 8, 2009
- FDA Inspection 576014 - Arevipharma GmbH - 2009-04-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 8, 2009

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