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www.fdanews.com/articles/141688-fda-warning-letter-prompts-closure-of-hiv-test-kit-maker

FDA Warning Letter Prompts Closure of HIV Test Kit Maker

November 11, 2011
OraWell USA, a short-lived devicemaker specializing in in vitro diagnostic test kits for HIV detection, has shut down after an FDA warning that its test kits were not cleared and its manufacturing processes violated GMPs.
The GMP Letter