# Aurisco Pharmaceutical Co., Ltd - Inspection Records

Source: https://www.keypedia.com/companies/aurisco-pharmaceutical-co-ltd/0c1b2448-eac7-44af-8316-098b271b404f

> Inspection records and compliance data for Aurisco Pharmaceutical Co., Ltd in Tiantai, -. Access full analysis and detailed observations.

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## Details

- Name: Aurisco Pharmaceutical Co., Ltd
- FEI Number: 3005793293
- City: Tiantai
- State: -
- Country Name: China
- Zip Code: -
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1269298 - Aurisco Pharmaceutical Co., Ltd - 2025-03-21](https://www.keypedia.com/records/fda_inspections/aurisco-pharmaceutical-co-ltd/56cc402c-35b9-4236-aac6-c38152a02249) — source: FDA, date: March 21, 2025
- [FDA Inspection 1269298 - Aurisco Pharmaceutical Co., Ltd - 2025-03-21](https://www.keypedia.com/records/fda_inspections/aurisco-pharmaceutical-co-ltd/ba5fc973-a92f-4a74-93d9-0c4671db2445) — source: FDA, date: March 21, 2025
- [FDA Inspection 1269298 - Aurisco Pharmaceutical Co., Ltd - 2025-03-21](https://www.keypedia.com/records/fda_inspections/aurisco-pharmaceutical-co-ltd/8d828596-9883-49ca-b716-84ae503266c2) — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2025
- [FDA Inspection 1269298 - Aurisco Pharmaceutical Co., Ltd - 2025-03-21](https://www.keypedia.com/records/fda_inspections/aurisco-pharmaceutical-co-ltd/75073d78-86c1-43c3-9a1c-72acfa138769) — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2025
- [FDA Inspection 1077584 - Aurisco Pharmaceutical Co., Ltd - 2018-11-30](https://www.keypedia.com/records/fda_inspections/aurisco-pharmaceutical-co-ltd/1d53a894-ba63-4395-b9b1-b1aa2bb491c5) — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2018
- [FDA Inspection 856482 - Aurisco Pharmaceutical Co., Ltd - 2013-11-15](https://www.keypedia.com/records/fda_inspections/aurisco-pharmaceutical-co-ltd/1ec94654-5fbc-4b9b-bc7e-56a82f41a162) — classification: No Action Indicated (NAI), source: FDA, date: November 15, 2013

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