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Home » FDA: Heparin Supplier’s Response to Form 483 Falls Short
FDA: Heparin Supplier’s Response to Form 483 Falls Short
February 1, 2011
The FDA has warned Scientific Protein Laboratories (SPL) that it could face legal action if it does not immediately correct a series of good manufacturing practice (GMP) violations cited during a July 28 to Sept. 3 inspection of its Waunakee, Wis., manufacturing plant.
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