FDA issued a Warning Letter to Daito Kasei Kogyo Co Ltd on 1/18/2018 as a result of this inspection.
483 Daito Kasei Kogyo Jul 2017

483 Daito Kasei Kogyo Jul 2017

Juan Jimenez Garcia FDA$119.00 - Available Now

FDA investigators audited the Daito Kasei Kogyo - Bizen, Japan facility and issued inspectional observations (via FDA 483) on 21 Jul 2017.

Product details

  • Category: Human Drugs
  • Inspection end: 21 Jul 2017
  • Location: Bizen, Japan
  • FEI: 1000223178
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