# FDA Inspection 568474 - Newmark, Inc. - March 04, 2009

Source: https://www.keypedia.com/records/fda_inspections/newmark-inc/08e49d80-822c-4332-8c11-5e99b89d2e63
Source feed: FDA_Inspections

> FDA Inspection 568474 for Newmark, Inc. on March 04, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 568474
- Company Name: Newmark, Inc.
- Inspection Date: 2009-03-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 827583 - 2013-04-11](https://www.keypedia.com/records/fda_inspections/newmark-inc/60613afd-b887-45ee-9540-6d727919e8f6)

Company: https://www.keypedia.com/companies/newmark-inc/14408a38-0d4d-475d-98e4-eb9c39aabf1c

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