# Interplex Medical  LLC – FDA Inspection, Sep 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 of Interplex Medical  LLC, September 20, 2023. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1029253 - 2017-10-17

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/amber-m-capello-jones/d34f92a0-d580-4028-9d31-c6cd7c13ce0f)
- Teresa K. Kastner

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