Aplicare Products, LLC

Form 483

Meriden, Connecticut, United StatesFEI 1220701Issued September 02, 2016

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 1220701.

Observations3

Issue DateSeptember 02, 2016

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Aplicare Products, LLC
Location: Meriden, Connecticut, United States
FEI Number: 1220701
Product Type: Devices
Issue Date: September 02, 2016
Country: United States

Inspection History, 2009 to 2021

NAI5

VAI3

OAI2

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

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Aplicare Products, LLC FDA Form 483, Meriden, Connecticut, September 2, 2016