FDA issued a Warning Letter to Smith & Nephew, Inc. on 6/11/2014 for a previous inspection.
483 Smith & Nephew Jan 2015

483 Smith & Nephew Jan 2015

Joshua Silvestri FDA$595.00 - Available Now

FDA investigators audited the Smith & Nephew - Saint Petersburg, FL, United States facility and issued 2 inspectional observations (via FDA 483) on 13 Jan 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 2
  • Inspection end: 13 Jan 2015
  • Location: Saint Petersburg, United States
  • FEI: 3006760724
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