Baxter 3/12/99 Catheters
2. Failure to validate production processes with a high degree of assurance where
the results of a process cannot be fully verified by subsequent inspection and test [21CFR 820.75). Specifically, your firm does not have sufficient documented evidence, that the Pulmonary Artery Catheter balloon forming, and the polyethylene (PVC)compounding processes meet their pre-determined specifications and quality
attributes.