KDL Precision Molding

Form 483FOIA Uncovered

Pacoima, California, United StatesFEI 3002941807Issued February 07, 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 3002941807.

Observations2

Issue DateFebruary 07, 2019

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: KDL Precision Molding
Location: Pacoima, California, United States
FEI Number: 3002941807
Product Type: Devices
Issue Date: February 07, 2019
Country: United States

Inspection History, 2013 to 2019

NAI1

VAI2

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

Act on This Form 483

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KDL Precision Molding FDA Form 483, Pacoima, California, February 7, 2019