# FDA Inspection 1180138 - Antarma LLC - September 23, 2022

Source: https://www.keypedia.com/records/fda_inspections/antarma-llc/0377fc98-6ab5-4e6e-bdc1-b50c73b1c901
Source feed: FDA_Inspections

> FDA Inspection 1180138 for Antarma LLC on September 23, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180138
- Company Name: Antarma LLC
- Inspection Date: 2022-09-23
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1180138 - 2022-09-23](https://www.keypedia.com/records/fda_inspections/antarma-llc/4b9e5ffc-9a7e-4b65-82db-303d5c43ae2d)
- [FDA Inspection 1094963 - 2019-06-07](https://www.keypedia.com/records/fda_inspections/antarma-llc/7fc2a7e9-10a5-46d6-9286-7f6cbe0f0084)
- [FDA Inspection 1094963 - 2019-06-07](https://www.keypedia.com/records/fda_inspections/antarma-llc/d3c1c9c4-8490-4510-bd32-1dac9aadefbf)

Company: https://www.keypedia.com/companies/antarma-llc/948a9867-eeb1-4711-b2b1-c2098d8603d7

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