# Aesica Pharmaceutical GmbH - Inspection Records

Source: https://www.keypedia.com/companies/aesica-pharmaceutical-gmbh/f804258b-606a-4c98-a131-7d238212ef12

> Inspection records and compliance data for Aesica Pharmaceutical GmbH in Monheim am Rhein, None. Access full analysis and detailed observations.

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## Details

- Name: Aesica Pharmaceutical GmbH
- FEI Number: 3002943189
- City: Monheim am Rhein
- State: None
- Country Name: Germany
- Address Line 1: Alfred-Nobel-Str. 10
- Zip Code: None

## Related Documents

- [FDA Inspection 1306304 - Aesica Pharmaceutical GmbH - 2024-09-12](https://www.keypedia.com/records/fda_inspections/aesica-pharmaceutical-gmbh/498b079d-5856-40d3-8ab3-acd08c3083ee) — source: FDA, date: September 12, 2024
- [FDA Inspection 1306304 - Aesica Pharmaceutical GmbH - 2024-09-12](https://www.keypedia.com/records/fda_inspections/aesica-pharmaceutical-gmbh/50b4ff3b-c8a7-4b8e-8f38-e84917ae532b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 12, 2024
- [FDA Inspection 1190265 - Aesica Pharmaceutical GmbH - 2021-07-01](https://www.keypedia.com/records/fda_inspections/aesica-pharmaceutical-gmbh/4f929909-5ccf-4d41-8ddc-e1541a47a86b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 1, 2021
- [FDA Inspection 1032046 - Aesica Pharmaceutical GmbH - 2017-09-20](https://www.keypedia.com/records/fda_inspections/aesica-pharmaceutical-gmbh/a581b7de-c091-46cc-b721-b39f2b8c47cf) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2017
- [FDA Inspection 866229 - Aesica Pharmaceutical GmbH - 2014-01-17](https://www.keypedia.com/records/fda_inspections/aesica-pharmaceutical-gmbh/b2a79b1e-b01a-49f4-a5d2-c659cc332b7a) — classification: No Action Indicated (NAI), source: FDA, date: January 17, 2014
- [FDA Inspection 759369 - Aesica Pharmaceutical GmbH - 2011-11-11](https://www.keypedia.com/records/fda_inspections/aesica-pharmaceutical-gmbh/6cc1eb00-373b-489f-8362-2f9f7cf09e41) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 11, 2011

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