FDA issued a Warning Letter to ASI Medical, Inc. on 1/23/2013 as a result of this inspection.
483 ASI Medical Dec 2011

483 ASI Medical Dec 2011

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FDA investigators audited the ASI Medical - Englewood, CO, United States facility and issued inspectional observations (via FDA 483) on 22 Dec 2011.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 22 Dec 2011
  • Location: Englewood, United States
  • FEI: 1000160293
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