# FDA Inspection 1218976 - Interplex Medical  LLC - September 20, 2023

Source: https://www.keypedia.com/records/fda_inspections/interplex-medical-llc/3bbb9af9-668b-46d7-acf5-2f95dbe63728
Source feed: FDA_Inspections

> FDA Inspection 1218976 for Interplex Medical  LLC on September 20, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1218976
- Company Name: Interplex Medical  LLC
- Inspection Date: 2023-09-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1029253 - 2017-10-17](https://www.keypedia.com/records/fda_inspections/interplex-medical-llc/c516b76c-f827-4e9b-bde6-fee7f3634734)

Company: https://www.keypedia.com/companies/interplex-medical-llc/1aa13bc1-94bc-4e3a-96db-00396095e78a

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