# SEAGEN INC. - Inspection Records

Source: https://www.keypedia.com/companies/seagen-inc/07c5dcb3-661e-4212-adfc-a00316850e38

> Inspection records and compliance data for SEAGEN INC. in Bothell, Washington. Access full analysis and detailed observations.

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## Details

- Name: SEAGEN INC.
- FEI Number: 3002781621
- City: Bothell
- State: Washington
- Country Name: United States
- Address Line 1: 2500 223rd St Se
- Zip Code: 98021

## Related Documents

- [483 - SEAGEN INC. - 2025-05-13](https://www.keypedia.com/records/483/seagen-inc/2c35d8cb-a857-4b8a-ad27-b43ba4571b46) — source: FDA, date: May 13, 2025
- [FDA Inspection 1272265 - SEAGEN INC. - 2025-05-13](https://www.keypedia.com/records/fda_inspections/seagen-inc/33d5bc76-b106-486b-aa5a-2ab3314b6690) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 13, 2025
- [FDA Inspection 1253880 - SEAGEN INC. - 2024-11-01](https://www.keypedia.com/records/fda_inspections/seagen-inc/7ea4e2b1-503a-4f33-9a11-47233fa9eb3c) — source: FDA, date: November 1, 2024
- [FDA Inspection 1253880 - SEAGEN INC. - 2024-11-01](https://www.keypedia.com/records/fda_inspections/seagen-inc/b545091b-3c12-4910-9279-7e680638617e) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2024
- [FDA Inspection 1236983 - SEAGEN INC. - 2024-05-02](https://www.keypedia.com/records/fda_inspections/seagen-inc/682be154-de32-470b-a13f-b4731c0a721e) — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2024
- [483 - SEAGEN INC. - 2022-06-10](https://www.keypedia.com/records/483/seagen-inc/ea221205-cb50-4ee9-9807-a41206c70bce) — source: FDA, date: June 10, 2022
- [FDA Inspection 1119141 - SEAGEN INC. - 2020-01-24](https://www.keypedia.com/records/fda_inspections/seagen-inc/571851d9-1666-4545-998b-65c7fb59d401) — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2020
- [EIR - SEAGEN INC. - 2019-10-04](https://www.keypedia.com/records/eir/seagen-inc/0d015a1c-7e6d-4cca-b8fc-f6f985a9e727) — source: FDA, date: October 4, 2019
- [FDA Inspection 1107250 - SEAGEN INC. - 2019-10-04](https://www.keypedia.com/records/fda_inspections/seagen-inc/b3cca369-aa91-4978-b493-726eaf2f80f0) — classification: No Action Indicated (NAI), source: FDA, date: October 4, 2019
- [FDA Inspection 1040735 - SEAGEN INC. - 2018-01-05](https://www.keypedia.com/records/fda_inspections/seagen-inc/a9eeec73-18d8-4016-8722-1d2352f0ff80) — classification: No Action Indicated (NAI), source: FDA, date: January 5, 2018
- [FDA Inspection 1011478 - SEAGEN INC. - 2017-05-01](https://www.keypedia.com/records/fda_inspections/seagen-inc/ac55515f-4f67-4756-8f43-566d0f1b6cd8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 1, 2017
- [FDA Inspection 930334 - SEAGEN INC. - 2015-06-09](https://www.keypedia.com/records/fda_inspections/seagen-inc/f108399b-7446-4e79-913f-5a8c24bdc6c9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 9, 2015
- [FDA Inspection 822857 - SEAGEN INC. - 2013-03-20](https://www.keypedia.com/records/fda_inspections/seagen-inc/8b9df84c-c3dc-4dcc-a575-f8d4ec874480) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 20, 2013

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