# FDA Inspection 1179020 - Syntermed, Inc. - August 11, 2022

Source: https://www.keypedia.com/records/fda_inspections/syntermed-inc/082780b4-4c5b-42f1-bfeb-1067fbbd6636
Source feed: FDA_Inspections

> FDA Inspection 1179020 for Syntermed, Inc. on August 11, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1179020
- Company Name: Syntermed, Inc.
- Inspection Date: 2022-08-11
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1179020 - 2022-08-11](https://www.keypedia.com/records/fda_inspections/syntermed-inc/f49186a9-f16a-4344-a386-70dfbf5bbb0c)
- [FDA Inspection 1064694 - 2018-05-23](https://www.keypedia.com/records/fda_inspections/syntermed-inc/1ed6f5a8-741d-4a1f-97ca-cadded90ef95)
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- [FDA Inspection 810182 - 2012-11-30](https://www.keypedia.com/records/fda_inspections/syntermed-inc/53d8aa20-a07d-4e26-a464-d32b1e5f36e3)

Company: https://www.keypedia.com/companies/syntermed-inc/a096f5b2-1bcd-4ce6-af9c-17cd1ce3f7b8

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