FDA issued a Warning Letter to Huestis Machine Corporation on 8/6/2013 as a result of this inspection.
483 Huestis Machine May 2013

483 Huestis Machine May 2013

Elizabeth Griffin FDA$119.00 - Available Now

FDA investigators audited the Huestis Machine - Bristol, RI, United States facility and issued 9 inspectional observations (via FDA 483) on 13 May 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 9
  • Inspection end: 13 May 2013
  • Location: Bristol, United States
  • FEI: 1219183
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