Keter Canada, Inc.

Form 483

MiltonFEI 3010508078Issued September 05, 2025

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 3010508078.

Observations12

Issue DateSeptember 05, 2025

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Keter Canada, Inc.
Location: Milton
FEI Number: 3010508078
Product Type: Devices
Issue Date: September 05, 2025
Country: N/A

Inspection History, 2022 to 2025

VAI1

OAI1

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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Keter Canada, Inc. FDA Form 483, Milton, September 5, 2025