# FDA Inspection 897083 - TeleMed Systems - September 30, 2014

Source: https://www.keypedia.com/records/fda_inspections/telemed-systems/0c46b399-7296-4fec-a610-c03e73d3bc9b
Source feed: FDA_Inspections

> FDA Inspection 897083 for TeleMed Systems on September 30, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 897083
- Company Name: TeleMed Systems
- Inspection Date: 2014-09-30
- 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/telemed-systems/e7ec5771-eeb5-49af-8c28-ed2821cfbc11

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