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Miyoshi America, Inc. — FDA Facility Profile

FEI 3009481791

Miyoshi America, Inc. is an FDA-registered facility (FEI 3009481791) located in Dayville, CT, US. Registered operations: API MANUFACTURE; LABEL; PACK. RegDataLab tracks 6 FDA inspections at this facility.

Facility Details

Location
Dayville, CT (US)
Registration Expires
December 31, 2026
Operations
API MANUFACTURE; LABEL; PACK
Source
decrs

Recent inspections

  • 1306728 (VAI Fri Feb 06 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1198326 (VAI Fri Jan 13 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1144549 (OAI Tue May 25 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 974319 (NAI Fri Jun 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 950532 (NAI Tue Nov 17 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 737348 (VAI Wed Jul 20 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources