FDA issued a Warning Letter to Advanced OrthoPro, Inc. on 5/18/2012 for a previous inspection.
483 Advanced OrthoPro Jul 2015

483 Advanced OrthoPro Jul 2015

Joseph Strelnik FDA$119.00 - Available Now

FDA investigators audited the Advanced OrthoPro - Indianapolis, IN, United States facility and issued 2 inspectional observations (via FDA 483) on 30 Jul 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 2
  • Inspection end: 30 Jul 2015
  • Location: Indianapolis, United States
  • FEI: 3007912159
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