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FDA Inspection 838341 — Rockledge Pharmaceutical Manufacturing LLC

Rockledge Pharmaceutical Manufacturing LLC — FEI 1000113139

The FDA completed an inspection of Rockledge Pharmaceutical Manufacturing LLC on June 20, 2013 in Rockledge, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 20, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockledge, FL (United States)

Facility

Other inspections at this facility

  • 1250752 (VAI Thu Apr 24 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1077088 (VAI Fri Jan 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 973786 (VAI Thu May 19 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 597735 (VAI Thu Jul 16 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources