# FDA Inspection 822820 - LDR Spine USA, Inc. - March 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/ldr-spine-usa-inc/68d48580-dbad-4a8d-896b-a9db8aab73e1
Source feed: FDA_Inspections

> FDA Inspection 822820 for LDR Spine USA, Inc. on March 15, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 822820
- Company Name: LDR Spine USA, Inc.
- Inspection Date: 2013-03-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ldr-spine-usa-inc/d2e885db-2f9e-4002-abdb-91b643b92184

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