FDA issued a Warning Letter to Hill-Rom, Inc. on 3/2/2012 for a later inspection.
483 Hill-Rom Jun 2007

483 Hill-Rom Jun 2007

Maribeth Niesen FDA$119.00 - Available Now

FDA investigators audited the Hill-Rom - Batesville, IN, United States facility and issued 5 inspectional observations (via FDA 483) on 21 Jun 2007.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 5
  • Inspection end: 21 Jun 2007
  • Location: Batesville, United States
  • FEI: 1824206
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