FDA issued a Warning Letter to X12 Co., LTD. on 3/23/2017 as a result of this inspection.
483 X12 Sep 2016

483 X12 Sep 2016

Cheryl Mccall FDA$119.00 - Available Now

FDA investigators audited the X12 - Sofia, Bulgaria facility and issued inspectional observations (via FDA 483) on 07 Sep 2016.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 07 Sep 2016
  • Location: Sofia, Bulgaria
  • FEI: 3009222666
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