# Gedeon Richter Nyrt. - Inspection Records

Source: https://www.keypedia.com/companies/gedeon-richter-nyrt/64f32cb7-f6af-4da0-b8b3-d2f6fee3c19b

> Inspection records and compliance data for Gedeon Richter Nyrt. in Budapest, None. Access full analysis and detailed observations.

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## Details

- Name: Gedeon Richter Nyrt.
- FEI Number: 3002806761
- City: Budapest
- State: None
- Country Name: Hungary
- Address Line 1: Gyomroi Ut 19-21
- Zip Code: None
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING, PACK

## Related Documents

- [FDA Inspection 1301414 - Gedeon Richter Nyrt. - 2025-07-04](https://www.keypedia.com/records/fda_inspections/gedeon-richter-nyrt/45d43648-04b6-4166-aadf-ec2c5720d20d) — source: FDA, date: July 4, 2025
- [FDA Inspection 1301414 - Gedeon Richter Nyrt. - 2025-07-04](https://www.keypedia.com/records/fda_inspections/gedeon-richter-nyrt/426e7063-68f2-49cf-9394-1c8bae7a3ebf) — classification: No Action Indicated (NAI), source: FDA, date: July 4, 2025
- [FDA Inspection 1207513 - Gedeon Richter Nyrt. - 2022-06-03](https://www.keypedia.com/records/fda_inspections/gedeon-richter-nyrt/396cd57e-900d-4d7f-ba84-deef78e8f82a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 3, 2022
- [FDA Inspection 1009633 - Gedeon Richter Nyrt. - 2017-03-03](https://www.keypedia.com/records/fda_inspections/gedeon-richter-nyrt/58e6d6f8-2023-4126-935d-de9fbe03334c) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2017
- [FDA Inspection 883062 - Gedeon Richter Nyrt. - 2014-05-23](https://www.keypedia.com/records/fda_inspections/gedeon-richter-nyrt/e1b80877-fb21-4ea5-99e3-2b784350c6aa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2014
- [FDA Inspection 738485 - Gedeon Richter Nyrt. - 2011-07-12](https://www.keypedia.com/records/fda_inspections/gedeon-richter-nyrt/7ae645f5-2929-44a4-9319-6f11f300bb26) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2011

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