FDA issued a Warning Letter to Instratek, Incorporated on 8/23/2012 as a result of this inspection.
483 Instratek Apr 2012

483 Instratek Apr 2012

Ellen Tave FDA$119.00 - Available Now

FDA investigators audited the Instratek - Houston, TX, United States facility and issued 9 inspectional observations (via FDA 483) on 24 Apr 2012.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 9
  • Inspection end: 24 Apr 2012
  • Location: Houston, United States
  • FEI: 1000118334
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