DPM USA Corp.

Form 483

Sweetwater, Florida, United StatesFEI 3001779742Issued December 07, 2012

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 3001779742.

Observations5

Issue DateDecember 07, 2012

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: DPM USA Corp.
Location: Sweetwater, Florida, United States
FEI Number: 3001779742
Product Type: Devices
Issue Date: December 07, 2012
Country: United States

Inspection History, 2012 to 2018

NAI1

VAI2

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

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DPM USA Corp. FDA Form 483, Sweetwater, Florida, December 7, 2012