# FDA Inspection 1019344 - Solventum US LLC - June 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 for Solventum US LLC on June 21, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1019344
- Company Name: Solventum US LLC
- Inspection Date: 2017-06-21
- 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 1248520 - 2024-09-06](https://www.keypedia.com/records/fda_inspections/solventum-us-llc/e2381e8a-a024-4379-9d51-06d823921aff)
- [FDA Inspection 1019344 - 2017-06-21](https://www.keypedia.com/records/fda_inspections/solventum-us-llc/0557bbc6-5712-47f5-9b7f-a3b7dd107e2c)
- [FDA Inspection 964790 - 2016-02-04](https://www.keypedia.com/records/fda_inspections/solventum-us-llc/cf1d895c-239e-4e18-9dcb-1aa6882a57a2)

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