FDA Inspection 1050929 — Rockline Industries, Inc

Rockline Industries, Inc — FEI 2129284

The FDA completed an inspection of Rockline Industries, Inc on May 4, 2018 in Sheboygan, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 4, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sheboygan, WI (United States)

Citations

IDCFRDescription
178721 CFR 211.80(a)Procedures To Be in Writing