Critical Cleaning

Critical Cleaning terminology describes: Processes used on parts that are used in critical process such as medical device fabrication, extremely small denier fibers, thin films, pharmaceutical applications, or any other application where biological and/or airborne particulate may interfere with the quality of the product.  Processes used to clean fragile or specialty designed parts where normal operations may prove to be damaging. Processes that comply with FDA or other Health or Environmental Agencies.

CFI can provide “critical cleaning & testing” services in a clean room environment or in a typical manufacturing setting.  Such processes include:

Processing

• Water, acidic & alkaline ultrasonic treatment
• DI Water flush
• Passivation
• Drying
• Packaging

Testing

• Water quality checks
• TOC (Total organic carbon)
• TSS (Total suspended solids)
• Bio-burden
• Air particulate count
• Visual inspection
• Microscopic inspection
• Bubble Point Testing
• Dry Air ∆P Testing
• Weighing

Other

• Customized packaging
• Customized labeling
• Customized data reporting
• Photographic documentation of microscopic inspection
• Customized handling of small or delicate items