# DMG America LLC dba Goldsmith & Revere, Inc. – FDA Inspection, Jan 29, 2013

Source: https://www.keypedia.com/records/fda_inspections/dmg-america-llc-dba-goldsmith-revere-inc/f4469103-e68d-470d-8a38-8379fa0768fe
Source feed: FDA_Inspections

> FDA inspection 816472 of DMG America LLC dba Goldsmith & Revere, Inc., January 29, 2013. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 816472
- Company Name: DMG America LLC dba Goldsmith & Revere, Inc.
- Inspection Date: 2013-01-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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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