Company
United StatesActavis LLC, Edison, NJ – FDA Inspections
Inspection records and compliance data for Actavis LLC in Edison, New Jersey. 6 FDA inspections on record, 1 Form 483, last inspected November 22, 2024.
Company Profile
This profile covers Actavis LLC based in Edison, New Jersey, United States.
FDA Inspection History
- FDA inspections
- 6
- OAI
- 0
- VAI
- 2
- NAI
- 4
- Form 483s
- 1
- Warning letters
- 0
First inspected January 27, 2012. Last inspected November 22, 2024.
Most cited issue areas
- Containers sampled so as to prevent contamination1 inspection
- Labeling and packaging improperly approved/released1 inspection
- Quarantined Drug Products Area1 inspection
FDA inspections (6)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| November 22, 2024 | NAI | Human Drugs · Drug Quality Assurance | 1256490 |
| August 8, 2019 | NAI | Human Drugs · Drug Quality Assurance | 1100659 |
| May 7, 2018 | VAI | Human Drugs · Drug Quality Assurance | 1050957 |
| July 7, 2016 | VAI | Human Drugs · Drug Quality Assurance | 978483 |
| October 29, 2013 | NAI | Human Drugs · Drug Quality Assurance | 854136 |
| January 27, 2012 | NAI | Human Drugs · Drug Quality Assurance | 764993 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Actavis LLC
FEI Number
3009017204
Address
47 Brunswick Ave, Edison, New Jersey 08817, United States
Country
United States
ID: 00e750d3-01ec-4f1d-8457-46a409935371