FDA issued a Warning Letter to Conair Corporation on 8/12/2013 as a result of this inspection.
483 Conair May 2013

483 Conair May 2013

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FDA investigators audited the Conair - Stamford, CT, United States facility and issued 8 inspectional observations (via FDA 483) on 31 May 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 8
  • Inspection end: 31 May 2013
  • Location: Stamford, United States
  • FEI: 1000121041
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