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FDA Inspection 949047 — Rockline Industries, Inc

Rockline Industries, Inc — FEI 2129284

The FDA completed an inspection of Rockline Industries, Inc on October 6, 2015 in Sheboygan, WI. 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
October 6, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sheboygan, WI (United States)

Facility

Other inspections at this facility

  • 1274598 (NAI Thu Jun 26 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1050929 (VAI Fri May 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 976464 (NAI Tue May 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 817293 (NAI Wed Feb 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 765470 (VAI Mon Jan 30 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources