# Mitsubishi Tanabe Pharma Development America, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/mitsubishi-tanabe-pharma-development-america-inc/f5e77e46-b625-4cdd-a44a-ecd7583b6baa

> Inspection records and compliance data for Mitsubishi Tanabe Pharma Development America, Inc. in Jersey City, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Mitsubishi Tanabe Pharma Development America, Inc.
- FEI Number: 3003777563
- City: Jersey City
- State: New Jersey
- Country Name: United States
- Address Line 1: 525 Washington Blvd Ste 400
- Zip Code: 07310

## Related Documents

- [FDA Inspection 1298296 - Mitsubishi Tanabe Pharma Development America, Inc. - 2025-09-18](https://www.keypedia.com/records/fda_inspections/mitsubishi-tanabe-pharma-development-america-inc/dceb2a25-e1ea-4e5b-a250-2f0f9fccf476) — source: FDA, date: September 18, 2025
- [FDA Inspection 1298296 - Mitsubishi Tanabe Pharma Development America, Inc. - 2025-09-18](https://www.keypedia.com/records/fda_inspections/mitsubishi-tanabe-pharma-development-america-inc/966fdd86-5f4d-4564-b692-4041fbe72ffd) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2025
- [483 - Mitsubishi Tanabe Pharma Development America, Inc. - 2021-10-15](https://www.keypedia.com/records/483/mitsubishi-tanabe-pharma-development-america-inc/40f73b79-76f1-4878-a034-b697a60dcaaa) — source: FDA, date: October 15, 2021
- [FDA Inspection 1155136 - Mitsubishi Tanabe Pharma Development America, Inc. - 2021-10-15](https://www.keypedia.com/records/fda_inspections/mitsubishi-tanabe-pharma-development-america-inc/f7044b8b-5d0a-4038-b5b4-93419bd38f76) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2021
- [FDA Inspection 857641 - Mitsubishi Tanabe Pharma Development America, Inc. - 2013-12-04](https://www.keypedia.com/records/fda_inspections/mitsubishi-tanabe-pharma-development-america-inc/24eb30a9-ccc6-44e7-bcfa-9e1a8da6556c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 4, 2013

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