# Solupharm Pharmazeutische Erzeugnisse Gmbh, Melsungen, Germany – FDA Inspections

Source: https://www.keypedia.com/companies/solupharm-pharmazeutische-erzeugnisse-gmbh/dd3d4b95-d76b-4afa-b430-f1dee1ebb184

> Inspection records and compliance data for Solupharm Pharmazeutische Erzeugnisse Gmbh in Melsungen. 5 FDA inspections on record, 1 Form 483, last inspected July 29, 2022.

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## Details

- Name: Solupharm Pharmazeutische Erzeugnisse Gmbh
- FEI Number: 3008255368
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK
- Address Line 1: Industriestr. 3
- City: Melsungen
- Country Name: Germany
- Address: Industriestr. 3, Melsungen, Germany
- Country: Germany

## Related Documents

- [FDA Inspection 1201236 - Solupharm Pharmazeutische Erzeugnisse Gmbh - 2022-07-29](https://www.keypedia.com/records/fda_inspections/solupharm-pharmazeutische-erzeugnisse-gmbh/8db235cb-7ffb-47bb-946e-c8ec8bc4830c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 29, 2022
- [FDA Inspection 1039841 - Solupharm Pharmazeutische Erzeugnisse Gmbh - 2018-02-02](https://www.keypedia.com/records/fda_inspections/solupharm-pharmazeutische-erzeugnisse-gmbh/9edd0188-33c6-468e-896a-043686310d51) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 2, 2018
- FDA Inspection 980047 - Solupharm Pharmazeutische Erzeugnisse Gmbh - 2016-06-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 21, 2016
- [FDA Inspection 897666 - Solupharm Pharmazeutische Erzeugnisse Gmbh - 2014-09-22](https://www.keypedia.com/records/fda_inspections/solupharm-pharmazeutische-erzeugnisse-gmbh/c908fb5d-c6bd-4cce-b87e-b0efe196fe69) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 22, 2014
- [FDA Inspection 756529 - Solupharm Pharmazeutische Erzeugnisse Gmbh - 2011-11-22](https://www.keypedia.com/records/fda_inspections/solupharm-pharmazeutische-erzeugnisse-gmbh/d8808045-bf69-4b84-811f-fe34bae87d15) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2011

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