Miyoshi America, Inc.

Form 483FOIA Uncovered

Dayville, ConnecticutFEI 3009481791Issued January 13, 2023

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3009481791.

ObservationsNot available

Issue DateJanuary 13, 2023

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Miyoshi America, Inc.
Location: Dayville, Connecticut
FEI Number: 3009481791
Product Type: Drugs
Issue Date: January 13, 2023
Country: United States

Inspection History, 2011 to 2026

NAI2

VAI3

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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Miyoshi America, Inc. FDA Form 483, Dayville, Connecticut, January 13, 2023