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FMI is an FDA and EPA registered facility that adheres to cGMPs throughout our process. Our quality system includes:
Packaging Types
  • Trained and qualified operating personnel supported by experienced quality technicians
  • Standard Operating Procedures (SOPs)
  • Lot number control – all materials are tracked by unique lot numbers at every stage of production
  • Fully documented batch records
  • Appropriate analysis at every stage of production
  • Outside laboratory support for microbiological testing and various other analyses
Our on-site analytical capabilities include, but are not limited to:
  • Gas Chromatography
  • FTIR
  • Refractive Index
  • Density/Specific Gravity
  • pH
  • Viscosity
  • Odor evaluation
  • Flash point
  • Color matching
  • Various Wet analyses
  • Freeze/Thaw