# FDA Inspection 670226 - DMG America LLC dba Goldsmith & Revere, Inc. - July 07, 2010

Source: https://www.keypedia.com/records/fda_inspections/dmg-america-llc-dba-goldsmith-revere-inc/56f59162-8a60-4ff3-9565-9bfe30a8a9ce
Source feed: FDA_Inspections

> FDA Inspection 670226 for DMG America LLC dba Goldsmith & Revere, Inc. on July 07, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 670226
- Company Name: DMG America LLC dba Goldsmith & Revere, Inc.
- Inspection Date: 2010-07-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/dmg-america-llc-dba-goldsmith-revere-inc/bc61e3c5-b5ee-4820-b2d5-c23655a2572c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7