FDA issued a Warning Letter to NeoChild LLC on 7/29/2008 for a previous inspection.
483 Neochild Feb 2010

483 Neochild Feb 2010

Margaret Annes FDA$119.00 - Available Now

FDA investigators audited the Neochild - Oklahoma City, OK, United States facility and issued inspectional observations (via FDA 483) on 04 Feb 2010.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 04 Feb 2010
  • Location: Oklahoma City, United States
  • FEI: 3006271008
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