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483
•Actavis Laboratories FL, Inc.•January 17, 2020

Actavis Laboratories FL, Inc. – FDA 483, Jan 17, 2020

Record Details

An FDA inspection of Actavis Laboratories FL, Inc. in Davie, FL, revealed significant deficiencies across its quality systems, facilities, equipment, and production controls. The firm failed to conduct timely investigations into deviations, maintain validated process hold times, provide adequate employee training, properly locate and qualify equipment, and ensure proper equipment calibration. These issues indicate a lack of control over manufacturing processes and potentially impact drug product quality.

Company
Actavis Laboratories FL, Inc.
Inspection date
January 17, 2020
Product type
drugs
Office
Office of Medical Device and Radiological Health Division II
People
  • Jessica L. Pressley (Pharmacy Compounding National Expert, Drug Specialist, Drug Specialist, Foreign Cadre)
  • Ileana Barreto-Petit
View Company Profile

ID · 7e4f8db5-e212-457c-8eb7-38d9605b8d57

Other documents for Actavis Laboratories FL, Inc.
  • 483 - 2025-11-18November 18, 2025
  • EIR - 2021-05-25May 25, 2021
  • 483 - 2021-05-25May 25, 2021
  • WARNING_LETTER - 2018-07-19July 19, 2018
  • 483 - 2018-07-19July 19, 2018

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