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FDA Inspection 611626 — Actavis South Atlantic LLC

Actavis South Atlantic LLC — FEI 3004090892

The FDA completed an inspection of Actavis South Atlantic LLC on August 19, 2009 in Sunrise, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 19, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sunrise, FL (United States)

Facility

Other inspections at this facility

  • 783911 (NAI Wed Apr 25 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 783901 (NAI Thu Apr 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 722033 (NAI Thu Apr 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources