FDA issued a Warning Letter to Airsep Corporation on 9/15/2008 for a previous inspection.
483 AirSep Jun 2011

483 AirSep Jun 2011

Michael Burd FDA, Nicholas Mendiola FDA$119.00 - Available Now

FDA investigators audited the AirSep - Amherst, NY, United States facility and issued inspectional observations (via FDA 483) on 29 Jun 2011.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 29 Jun 2011
  • Location: Amherst, United States
  • FEI: 1319044
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