AirQ
Industrial
- Mar 6, 2007
- 1
Trying to benchmark 1) What type of documentation is created, and action taken, when a leak exceeding 0.01% during integrity testing (as with PAO) of a HEPA filter is detected? 2) If you do not respond to a >0.01% leak then at what % leak level do you start addressing documentation as investigation reports relating to the leak's impact on the product manufactured? Welcome all responses; however particularly interested in Pharmaceutical Manufacturing.