# TTY Biopham Company Ltd (Chung-Li Factory) - Inspection Records

Source: https://www.globalkeysolutions.net/companies/tty-biopham-company-ltd-chung-li-factory/ae797824-cd7b-494f-8ea5-27e29e23a334

> Inspection records and compliance data for TTY Biopham Company Ltd (Chung-Li Factory) in Chung-Li, -. Access full analysis and detailed observations.

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## Details

- Name: TTY Biopham Company Ltd (Chung-Li Factory)
- FEI Number: 3005054986
- City: Chung-Li
- State: -
- Country Name: United Kingdom
- Zip Code: -
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

- [FDA Inspection 1271715 - TTY Biopham Company Ltd (Chung-Li Factory) - 2025-05-02](https://www.globalkeysolutions.net/records/fda_inspections/tty-biopham-company-ltd-chung-li-factory/92b1a8a4-7db4-4548-8a07-3fd267ed59da) — source: FDA, date: May 2, 2025
- [FDA Inspection 1271715 - TTY Biopham Company Ltd (Chung-Li Factory) - 2025-05-02](https://www.globalkeysolutions.net/records/fda_inspections/tty-biopham-company-ltd-chung-li-factory/855cb05c-7f30-4a6e-9ebf-42ba9cc94585) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 2, 2025
- [FDA Inspection 1074092 - TTY Biopham Company Ltd (Chung-Li Factory) - 2018-11-16](https://www.globalkeysolutions.net/records/fda_inspections/tty-biopham-company-ltd-chung-li-factory/be2cbaec-5bea-4caa-ab8c-694abd001eef) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2018
- [FDA Inspection 965256 - TTY Biopham Company Ltd (Chung-Li Factory) - 2016-03-18](https://www.globalkeysolutions.net/records/fda_inspections/tty-biopham-company-ltd-chung-li-factory/2d29c390-c762-4e55-8cfb-84bff92ddf5f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2016
- [FDA Inspection 851466 - TTY Biopham Company Ltd (Chung-Li Factory) - 2013-09-27](https://www.globalkeysolutions.net/records/fda_inspections/tty-biopham-company-ltd-chung-li-factory/e8cad5a7-4b9e-4e6c-9f79-5556ba2031c6) — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2013

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