# MEDA Manufacturing GmbH - Inspection Records

Source: https://www.globalkeysolutions.net/companies/meda-manufacturing-gmbh/9dee9c01-de98-4a5e-9ab5-48a473581f49

> Inspection records and compliance data for MEDA Manufacturing GmbH in Cologne, None. Access full analysis and detailed observations.

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## Details

- Name: MEDA Manufacturing GmbH
- FEI Number: 3002808393
- City: Cologne
- State: None
- Country Name: Germany
- Address Line 1: Neurather Ring 1
- Zip Code: None

## Related Documents

- [FDA Inspection 1024520 - MEDA Manufacturing GmbH - 2017-09-07](https://www.globalkeysolutions.net/records/fda_inspections/meda-manufacturing-gmbh/6bf59010-b425-411e-9913-f2f01e5ef611) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 7, 2017
- [FDA Inspection 990063 - MEDA Manufacturing GmbH - 2016-09-09](https://www.globalkeysolutions.net/records/fda_inspections/meda-manufacturing-gmbh/ef5a7f7c-b8fd-4942-a465-5a51c3695dbb) — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2016
- [FDA Inspection 872188 - MEDA Manufacturing GmbH - 2013-11-22](https://www.globalkeysolutions.net/records/fda_inspections/meda-manufacturing-gmbh/9a7d7df6-40ea-47ef-8c0d-0b3c2b4f1f32) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2013
- [FDA Inspection 872188 - MEDA Manufacturing GmbH - 2013-11-22](https://www.globalkeysolutions.net/records/fda_inspections/meda-manufacturing-gmbh/d7ef23a0-3bba-447e-b3a9-609336cc6749) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2013
- [FDA Inspection 560082 - MEDA Manufacturing GmbH - 2009-01-30](https://www.globalkeysolutions.net/records/fda_inspections/meda-manufacturing-gmbh/f833a0e2-db7f-4aa1-8573-7bf870bec38d) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2009
- [FDA Inspection 560082 - MEDA Manufacturing GmbH - 2009-01-30](https://www.globalkeysolutions.net/records/fda_inspections/meda-manufacturing-gmbh/7fe1e26a-823c-4bf2-8002-527cd4164bcf) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2009

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