FDA issued a Warning Letter to Pinook-USA on 6/14/2012 for a previous inspection.
483 Pinook USA Mar 2013

483 Pinook USA Mar 2013

Angela Glenn FDA, Lisa Warner FDA$119.00 - Available Now

FDA investigators audited the Pinook USA - Orlando, FL, United States facility and issued 7 inspectional observations (via FDA 483) on 01 Mar 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 7
  • Inspection end: 01 Mar 2013
  • Location: Orlando, United States
  • FEI: 3008113239
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