FDA issued a Warning Letter to Whitehall/Div of Acorn Engineering Co on 7/12/2017 as a result of this inspection.
483 WHITEHALL A DIVISION OF ACORN ENGINEERING CO. Mar 2017

483 WHITEHALL A DIVISION OF ACORN ENGINEERING CO. Mar 2017

Donna Besone FDA$119.00 - Available Now

FDA investigators audited the WHITEHALL A DIVISION OF ACORN ENGINEERING CO. - City of Industry, CA, United States facility and issued inspectional observations (via FDA 483) on 23 Mar 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 23 Mar 2017
  • Location: City of Industry, United States
  • FEI: 1000150265
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