Day

April 3, 1996
Barton Carey Medical Products 4/3/96 our Investigator determined that your firm manufactures vascular and burn compression garments. These garments are devices as defined by Section 201(h) of the Federal Food, Drug and Cosmetic Act (the Act). The Inspection revealed that your devices are adulterated in that, the methods used in, or the facilities or controls...
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62304, FDA, and Emerging Standards for Medical Device and HealthIT
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Dates:  June 2-4, 2020
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