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Home » GMP Warning to Devicemaker Sets Deadlines for Third-Party Audit
GMP Warning to Devicemaker Sets Deadlines for Third-Party Audit
September 27, 2013
In a rare use of its powers, the FDA is requiring a California devicemaker to get a third-party audit of corrections relating to a slew of serious manufacturing and quality assurance deficiencies and verify the audit to the agency by March 1, 2014.