IQ PRODUCTS B.V.

Form 483FOIA Uncovered

Groningen, -, NetherlandsFEI 3002807541Issued July 17, 2019

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 3002807541.

Observations3

Issue DateJuly 17, 2019

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: IQ PRODUCTS B.V.
Location: Groningen, -, Netherlands
FEI Number: 3002807541
Product Type: Devices
Issue Date: July 17, 2019
Country: Netherlands

Inspection History, 2019 to 2026

NAI1

VAI2

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

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IQ PRODUCTS B.V. FDA Form 483, Groningen, July 17, 2019