# Solventum US LLC – FDA Inspection, Jun 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/solventum-us-llc/9fab0d34-5cd4-4771-8aaf-275cab1a6856
Source feed: FDA_Inspections

> FDA inspection 1019344 of Solventum US LLC, June 21, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1019344
- Company Name: Solventum US LLC
- Inspection Date: 2017-06-21
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1248520 - 2024-09-06](https://www.keypedia.com/records/fda_inspections/solventum-us-llc/e2381e8a-a024-4379-9d51-06d823921aff)
- FDA Inspection 964790 - 2016-02-04

## Related Officers

- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)

Company: https://www.keypedia.com/companies/solventum-us-llc/8195e7c6-5daf-4fbd-817a-9380b229bbcc

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