FDA issued a Warning Letter to Puretone Ltd. on 4/10/2009 for a later inspection.
483 Puretone Mar 2001

483 Puretone Mar 2001

Robert Ruff FDA$119.00 - Available Now

FDA investigators audited the Puretone - Rochester, United Kingdom facility and issued inspectional observations (via FDA 483) on 07 Mar 2001.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 07 Mar 2001
  • Location: Rochester, United Kingdom
  • FEI: 3002808722
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