# Millennium Pharmaceuticals Inc., Cambridge, MA – FDA Inspections

Source: https://www.keypedia.com/companies/millennium-pharmaceuticals-inc/df0887e9-e4d2-4ad0-8b1c-31f6bc3e9b92

> Inspection records and compliance data for Millennium Pharmaceuticals Inc. in Cambridge, Massachusetts. 7 FDA inspections on record, last inspected April 13, 2016.

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## Details

- Name: Millennium Pharmaceuticals Inc.
- FEI Number: 1000513221
- Address Line 1: 40 Landsdowne St
- City: Cambridge
- State: Massachusetts
- Zip Code: 02139
- Country Name: United States
- Address: 40 Landsdowne St, Cambridge, Massachusetts 02139, United States
- Country: United States

## Related Documents

- FDA Inspection 971665 - Millennium Pharmaceuticals Inc. - 2016-04-13 — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2016
- FDA Inspection 948448 - Millennium Pharmaceuticals Inc. - 2015-10-21 — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2015
- [FDA Inspection 894268 - Millennium Pharmaceuticals Inc. - 2014-08-15](https://www.keypedia.com/records/fda_inspections/millennium-pharmaceuticals-inc/de34b7ef-fcdb-4c81-91a4-9cf63fde7ffa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 15, 2014
- FDA Inspection 860615 - Millennium Pharmaceuticals Inc. - 2013-12-23 — classification: No Action Indicated (NAI), source: FDA, date: December 23, 2013
- FDA Inspection 808979 - Millennium Pharmaceuticals Inc. - 2012-11-30 — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2012
- [FDA Inspection 756510 - Millennium Pharmaceuticals Inc. - 2011-12-16](https://www.keypedia.com/records/fda_inspections/millennium-pharmaceuticals-inc/26c2face-15e9-4bd5-8c75-11018948ea82) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 16, 2011
- FDA Inspection 602517 - Millennium Pharmaceuticals Inc. - 2009-08-05 — classification: No Action Indicated (NAI), source: FDA, date: August 5, 2009
- FDA Inspection 602517 - Millennium Pharmaceuticals Inc. - 2009-08-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 5, 2009

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