# Nuvisan GmbH, Neu-Ulm, Germany – FDA Inspections

Source: https://www.keypedia.com/companies/nuvisan-gmbh/d25cfba4-0736-40b1-a157-52de725d5cc4

> Inspection records and compliance data for Nuvisan GmbH in Neu-Ulm. 5 FDA inspections on record, 1 Form 483, last inspected October 17, 2024.

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## Details

- Name: Nuvisan GmbH
- FEI Number: 3002809479
- Business Operations: API/FDF ANALYTICAL TESTING, CLINICAL BIOEQUIVALENCE OR BIOAVAILABILITY STUDY
- Address Line 1: Wegenerstr. 13
- City: Neu-Ulm
- Country Name: Germany
- Address: Wegenerstr. 13, Neu-Ulm, Germany
- Country: Germany

## Related Documents

- FDA Inspection 1288880 - Nuvisan GmbH - 2024-10-17 — source: FDA, date: October 17, 2024
- FDA Inspection 1288880 - Nuvisan GmbH - 2024-10-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 17, 2024
- FDA Inspection 1160058 - Nuvisan GmbH - 2020-02-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2020
- [FDA Inspection 1060551 - Nuvisan GmbH - 2018-06-08](https://www.keypedia.com/records/fda_inspections/nuvisan-gmbh/65187590-1574-44e2-9346-9623acaaf1c2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 8, 2018
- FDA Inspection 891842 - Nuvisan GmbH - 2014-07-25 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 25, 2014
- FDA Inspection 788970 - Nuvisan GmbH - 2012-05-16 — classification: No Action Indicated (NAI), source: FDA, date: May 16, 2012

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