Daily Medical Products, Inc.

Form 483

Plymouth, Minnesota, United StatesFEI 2083299Issued May 05, 2011

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 2083299.

Observations4

Issue DateMay 05, 2011

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Daily Medical Products, Inc.
Location: Plymouth, Minnesota, United States
FEI Number: 2083299
Product Type: Devices
Issue Date: May 05, 2011
Country: United States

Inspection History, 2011 to 2023

NAI3

VAI1

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

Act on This Form 483

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Daily Medical Products, Inc. FDA Form 483, Plymouth, Minnesota, May 5, 2011