# Takeda Pharmaceutical Company Limited - Inspection Records

Source: https://www.keypedia.com/companies/takeda-pharmaceutical-company-limited/4611dabc-52f7-4b4a-96bf-4196e34a7c2b

> Inspection records and compliance data for Takeda Pharmaceutical Company Limited in Round Lake, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Takeda Pharmaceutical Company Limited
- FEI Number: 3012385969
- City: Round Lake
- State: Illinois
- Country Name: United States
- Address Line 1: 25212 W Il Route 120
- Zip Code: 60073

## Related Documents

- [483 - Takeda Pharmaceutical Company Limited - 2025-11-26](https://www.keypedia.com/records/483/takeda-pharmaceutical-company-limited/e314f461-7a2b-42e9-9181-710be64dee9c) — source: FDA, date: November 26, 2025
- [FDA Inspection 1293098 - Takeda Pharmaceutical Company Limited - 2025-11-26](https://www.keypedia.com/records/fda_inspections/takeda-pharmaceutical-company-limited/1a77ba55-396a-4912-81d2-ff91a8e53f0c) — source: FDA, date: November 26, 2025
- [483 - Takeda Pharmaceutical Company Limited - 2022-09-15](https://www.keypedia.com/records/483/takeda-pharmaceutical-company-limited/4e49acd1-ce68-49ee-bfe4-8266281bdf7c) — source: FDA, date: September 15, 2022
- [FDA Inspection 1179911 - Takeda Pharmaceutical Company Limited - 2022-09-15](https://www.keypedia.com/records/fda_inspections/takeda-pharmaceutical-company-limited/e47449e5-f80c-46dd-b63d-6271b697efff) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 15, 2022
- [FDA Inspection 1179911 - Takeda Pharmaceutical Company Limited - 2022-09-15](https://www.keypedia.com/records/fda_inspections/takeda-pharmaceutical-company-limited/a52b6998-81c9-47c8-8868-df456fa2bcba) — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2022
- [FDA Inspection 1103189 - Takeda Pharmaceutical Company Limited - 2019-09-25](https://www.keypedia.com/records/fda_inspections/takeda-pharmaceutical-company-limited/f815b5da-2d6a-4e03-8688-006a8fbebf36) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 25, 2019

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