COMPANY FAILS TO REPLY TO FORM FDA 483 FROM JULY 2012 AUDIT Compliance Products, St. Louis, MO was audited by the Kansas City office of the FDA from July 16-20, 2012.  Following the audit, a total of eight Observations were issued.  As of the date of the Warning Letter, no response had been received by the FDA.  Many of the Observations represented recurring Observations – … [Read more...]