Baxter Healthcare Corporation Facility Gets Another FDA Warning Letter

After conducting inspections at Baxter Healthcare Corp.'s Round Lake, IL, facility, FDA has issued another Warning Letter regarding the plant. The latest letter stems from inspections that were conducted in July and August, 2013. The Warning Letter, dated January 17 but not posted on the FDA website until earlier this month, cites Good Manufacturing Practice deficiencies in the manufacture of three devices, and charges that the company has not properly addressed five deficiencies noted in a 2012 Warning Letter.

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