# Actavis Laboratories FL, Inc., Sunrise, FL – FDA Inspections

Source: https://www.keypedia.com/companies/actavis-laboratories-fl-inc/7c50db23-6cc7-4100-bc80-c02d3aa7f85a

> Inspection records and compliance data for Actavis Laboratories FL, Inc. in Sunrise, Florida. 5 FDA inspections on record, 1 Form 483, last inspected April 11, 2025.

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## Details

- Name: Actavis Laboratories FL, Inc.
- FEI Number: 3003937591
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING, PACK
- Address Line 1: 13900 Nw 2nd St Bldg A
- City: Sunrise
- State: Florida
- Zip Code: 33325
- Country Name: United States
- Address: 13900 Nw 2nd St Bldg A, Sunrise, Florida 33325, United States
- Country: United States

## Related Documents

- [FDA Inspection 1265179 - Actavis Laboratories FL, Inc. - 2025-04-11](https://www.keypedia.com/records/fda_inspections/actavis-laboratories-fl-inc/69e0dda8-2189-4591-b393-22e3c51bada3) — source: FDA, date: April 11, 2025
- FDA Inspection 1265179 - Actavis Laboratories FL, Inc. - 2025-04-11 — classification: No Action Indicated (NAI), source: FDA, date: April 11, 2025
- [483 - Actavis Laboratories FL, Inc. - 2017-12-01](https://www.keypedia.com/records/483/actavis-laboratories-fl-inc/464aa95a-8c29-407d-a49e-c70979c2693f) — source: FDA, date: December 1, 2017
- [FDA Inspection 1033874 - Actavis Laboratories FL, Inc. - 2017-12-01](https://www.keypedia.com/records/fda_inspections/actavis-laboratories-fl-inc/fcb54fe7-be95-4eae-814a-b6ebadbee949) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 1, 2017
- FDA Inspection 957324 - Actavis Laboratories FL, Inc. - 2016-01-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 14, 2016
- FDA Inspection 864453 - Actavis Laboratories FL, Inc. - 2014-01-30 — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2014
- FDA Inspection 638536 - Actavis Laboratories FL, Inc. - 2010-01-14 — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2010

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