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General FAQ’s

Other Questions:

How does Oxipack contribute to maintaining Acceptable Quality Levels (AQL)?

What is ASTM F2338 and why is it important for a leaktest?

What defines a leak? And how do we know if our packaging is leaking?

How can I get a demo of Oxipack’s leak detection machines?

How can I purchase an Oxipack leak detection machine?

How accurate are Oxipack’s leak detection machines?

Are Oxipack's leak detection methods safe for all types of products?

How does the food packaging industry maintain product freshness and safety through leak detection methods?

Can Oxipack's leak detector solutions detect leaks in packaging of any size or shape?

What makes Oxipack’s leak detection methods unique?

What methods are employed for a leaktest in pharmaceutical packaging, and how do they contribute to ensuring product safety?

How does the pharmaceutical packaging industry ensure the integrity of container closures to meet the acceptable quality level (AQL)?

What methods are commonly employed in pharmaceutical packaging quality control to ensure the integrity of sealed containers?

How can I ensure the integrity of our sealed packages within our production environment?

What is vacuum decay, and how does Oxipack utilize this method in leak detection?

What is a bubble test and how does it work?

What are the different types of seal integrity test methods used in the packaging industry?

What method complies with vacuum decay, and what does it entail for the evaluation of packaging?

How does Oxipack contribute to maintaining Acceptable Quality Levels (AQL)?

The Acceptable Quality Level (AQL) is a critical benchmark in quality control that defines the maximum number of defective items considered acceptable during random sampling. Oxipack's leak detection systems are engineered to deliver high-precision testing, helping manufacturers maintain AQL standards by swiftly identifying and rejecting packages with leaks, thereby ensuring product integrity and consumer safety.