# Actavis LLC - Inspection Records

Source: https://www.keypedia.com/companies/actavis-llc/00e750d3-01ec-4f1d-8457-46a409935371

> Inspection records and compliance data for Actavis LLC in Edison, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Actavis LLC
- FEI Number: 3009017204
- City: Edison
- State: New Jersey
- Country Name: United States
- Address Line 1: 47 Brunswick Ave
- Zip Code: 08817
- Business Operations: PACK

## Related Documents

- [FDA Inspection 1256490 - Actavis LLC - 2024-11-22](https://www.keypedia.com/records/fda_inspections/actavis-llc/11538837-baed-4e11-b669-f61c3fdd7c1e) — source: FDA, date: November 22, 2024
- [FDA Inspection 1256490 - Actavis LLC - 2024-11-22](https://www.keypedia.com/records/fda_inspections/actavis-llc/a1be8aa6-2f19-4e00-97cb-827c70628f6d) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2024
- [FDA Inspection 1100659 - Actavis LLC - 2019-08-08](https://www.keypedia.com/records/fda_inspections/actavis-llc/6eefc3d7-1227-4f40-8dae-5bb7b408315e) — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2019
- [FDA Inspection 1050957 - Actavis LLC - 2018-05-07](https://www.keypedia.com/records/fda_inspections/actavis-llc/38794933-e9f1-46d8-8f94-423a0137a9e1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 7, 2018
- [FDA Inspection 978483 - Actavis LLC - 2016-07-07](https://www.keypedia.com/records/fda_inspections/actavis-llc/47c36661-6b84-4639-bcf5-91043fec7fe9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 7, 2016
- [FDA Inspection 854136 - Actavis LLC - 2013-10-29](https://www.keypedia.com/records/fda_inspections/actavis-llc/6470f55e-0e25-4c66-9f4e-0c3e60941062) — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2013
- [FDA Inspection 764993 - Actavis LLC - 2012-01-27](https://www.keypedia.com/records/fda_inspections/actavis-llc/bf808326-61ef-4a0e-ac67-2665a7d8b9ac) — classification: No Action Indicated (NAI), source: FDA, date: January 27, 2012

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