FDA issued a Warning Letter to 86 Harriet Ave Corporation DBA General Devices on 6/1/2016 as a result of this inspection.
483 86 Harriet Ave DBA General Devices Jun 2015

483 86 Harriet Ave DBA General Devices Jun 2015

Li Li FDA$119.00 - Available Now

FDA investigators audited the 86 Harriet Ave DBA General Devices - Ridgefield, NJ, United States facility and issued inspectional observations (via FDA 483) on 11 Jun 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 11 Jun 2015
  • Location: Ridgefield, United States
  • FEI: 2244646
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