FDA issued a Warning Letter to Hammill Manufacturing Company on 1/6/2009 for a previous inspection.
483 Hammill Manufacturing Company Sep 2009

483 Hammill Manufacturing Company Sep 2009

Michael Larson FDA$119.00 - Available Now

FDA investigators audited the Hammill Manufacturing Company - Maumee, OH, United States facility and issued inspectional observations (via FDA 483) on 02 Sep 2009.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 02 Sep 2009
  • Location: Maumee, United States
  • FEI: 3000215103
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