DX PRODUCTS LIMITED

Form 483FOIA Uncovered

Horbury Wakefield, -, United KingdomFEI 3010386378Issued November 03, 2022

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 3010386378.

Observations4

Issue DateNovember 03, 2022

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: DX PRODUCTS LIMITED
Location: Horbury Wakefield, -, United Kingdom
FEI Number: 3010386378
Product Type: Devices
Issue Date: November 03, 2022
Country: United Kingdom

Inspection History, 2017 to 2026

NAI1

VAI2

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

Act on This Form 483

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DX PRODUCTS LIMITED FDA Form 483, Horbury Wakefield, November 3, 2022