logo

Compressed Air Viable Counts

aksharvalidation.com > Compressed Air Viable Counts

All Service

Compressed Air Viable Counts

Compressed air used in cleanrooms, pharmaceutical production, and food processing must be microbiologically clean to prevent contamination. Viable particles, unlike non-viable ones, are living microorganisms (such as bacteria, yeast, or mold) that pose a serious risk to product sterility and patient safety. Our Compressed Air Viable Count testing service is designed to detect and quantify microbial contamination in compressed air systems. Using specialized microbial impaction samplers and agar plates, we assess the bioburden level in your compressed air, helping ensure compliance with ISO 8573-7, WHO, EU GMP, and USFDA standards.

Why Compressed Air Viable Count Testing Matters


  • ✅ Prevents microbial contamination of sterile products

  • ✅ Ensures compliance with cleanroom classification and GMP guidelines

  • ✅ Supports risk assessment and contamination control strategies

  • ✅ Identifies breaches in filtration and sterilization processes

What We Detect


  • Bacteria

  • Yeasts

  • Molds

  • Other viable microorganisms present in compressed air

Industries We Serve


  • Pharmaceuticals & Biotechnology

  • Medical Device Manufacturing

  • Food & Beverage Processing

  • Hospitals & Healthcare Facilities

  • Cleanroom Environments

Ensure your compressed air meets the highest microbiological standards.
Schedule your Viable Count Testing today and maintain confidence in your clean air systems.