Veltek Associates, Inc.

Veltek Associates, Inc. is an 180,000 sq. ft. EPA and FDA registered manufacturing facility that focuses our products and services in assisting in the control of contamination in Class 100 to Class 100,000 areas. The five divisions of VAI and provide the ability to capture and identify contamination that may exist in pharmaceutical and biotechnology operations and assure its timely demise.

VAI's Sterile Chemical Manufacturing Division (SCMD) manufactures a complete range of pharmaceutical grade chemicals and disinfectants including DECON-AHOL™ Sterile Isopropyl Alcohol with WFI, STER-AHOL™ Denatured Ethyl Alcohol, DECON-PHENE™ (Sterile Phenolic), DECON-PHASE™ (Sterile Phenolic), DECON-CYCLE (Sterile Low pH Phenolic), DECON-Clean™ (Residue Remover), HYPO-CHLOR™ (5.25%, 0.52% and 0.25% Sterile Bleach), STERI-PEROX™ (3% and 6% Sterile Hydrogen Peroxide), STERI-WATER™ (Sterile Purified Water, USP), DECON-SPORE™ 100 and 200 (Sterile Peracitic Acid/Peroxide), STERI-OIL™ (Sterile Gear Oil), STERI-GREASE™ (Sterile White Grease), STERI-DEGREASE™ (Sterile Degreaser), STERI-SILICON™ (Sterile Food Grade Silicion), STERI-SIL 100 (Medical Grade Silicone) and STEEL-BRIGHT™ (Sterile Stainless Cleaner).

VAI Laboratories provides a complete range of microbiological testing services focusing on antimicrobial effectiveness testing as done via Time Contact Kill Studies, Time Contact Kill Studies on Varying Surfaces and AOAC Protocol Testing. VAI Laboratories also incorportaes complete microbial indentification services via fatty acid and genetic sequencing testing.

VAI's Environmental Control Monitoring Division (ECMD) manufactures the SMA™ Microbial Air Sampler for Portable and Multi Location Viable Air Testing. ECMD also manufactures the Helmke-Yeich™ Tumble Drum Tester and the Variable Temperature Controller capable of sampling for airborne particulate in ovens up to 500°C.

VAI's Disposable Products Manufacturing Division (DPMD) manufactures a complete range of disposable garments, wipers and facial barriers that are manufactured within a clean room from beginning to end.

VAI's Contract Packaging Manufacturing Division provides complete cGMP manufacturing operations and GLP laboratory services for specialty production as required by pharmaceutical and biotechnology organizations.

VAI Laboratories provides a complete range of testing services relating to the implementation of disinfecting agents and the implementation of sterile components. These services include; AOAC protocol testing, Time contact kill studies, complete disinfectant validation services, component sterility validation and on-site training services.