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Ishihara Sangyo Kaisha, Ltd. — FDA Facility Profile

FEI 3002807309

Ishihara Sangyo Kaisha, Ltd. is an FDA-registered facility (FEI 3002807309) located in Mie 510-0842, JP. Registered operations: API MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

Facility Details

Location
Mie 510-0842 (JP)
Registration Expires
December 31, 2026
Operations
API MANUFACTURE
Source
decrs

Recent inspections

  • 1181874 (VAI Fri Sep 09 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1028577 (VAI Fri Sep 08 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 895933 (VAI Fri Sep 05 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 747053 (VAI Fri Sep 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Import refusals

  • 221-6058468-0/1/1 (Tue Sep 29 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 221-6058468-0/2/1 (Tue Sep 29 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources