FDA issued a Warning Letter to Wonjin Mulsan Co., Ltd. on 7/31/2013 as a result of this inspection.
483 Wonjin Mulsan Apr 2013

483 Wonjin Mulsan Apr 2013

Thai Duong FDA$119.00 - Available Now

FDA investigators audited the Wonjin Mulsan - Incheon, Korea (the Republic of) facility and issued 5 inspectional observations (via FDA 483) on 04 Apr 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 5
  • Inspection end: 04 Apr 2013
  • Location: Incheon, Korea (the Republic of)
  • FEI: 3006797972
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