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The FDA was also seeking additional information regarding controls and specifications regarding the manufacturing, packaging and sterilization of ILUVIEN because the FDA had observed deficiencies in current good manufacturing practices (cGMP) during its facility inspections of two of Alimera's third-party manufacturers. The FDA has issued letters to both of these third-party manufacturers indicating that the inspections are now closed. Alimera believes that no further action is required and expects to include this information in the response it plans to file with the FDA by May 13, 2011.