HertART ApS

Form 483

Vastra Frolunda, -, SwedenFEI 3008524469Issued March 21, 2018

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 3008524469.

Observations7

Issue DateMarch 21, 2018

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: HertART ApS
Location: Vastra Frolunda, -, Sweden
FEI Number: 3008524469
Product Type: Devices
Issue Date: March 21, 2018
Country: Sweden

Inspection History, 2015 to 2023

NAI1

VAI2

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

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HertART ApS FDA Form 483, Vastra Frolunda, March 21, 2018