FDA issued a Warning Letter to Hammill Manufacturing Company on 1/6/2009 as a result of this inspection.
483 Hammill Manufacturing Company Nov 2008

483 Hammill Manufacturing Company Nov 2008

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FDA investigators audited the Hammill Manufacturing Company - Maumee, OH, United States facility and issued inspectional observations (via FDA 483) on 10 Nov 2008.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 10 Nov 2008
  • Location: Maumee, United States
  • FEI: 3000215103
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