# FDA Inspection 1052326 - DPM USA Corp. - February 28, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/dpm-usa-corp/b7ea4e9b-8d08-48e2-af04-5494571090b4
Source feed: FDA_Inspections

> FDA Inspection 1052326 for DPM USA Corp. on February 28, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1052326
- Company Name: DPM USA Corp.
- Inspection Date: 2018-02-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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Company: https://www.globalkeysolutions.net/companies/dpm-usa-corp/836cd82a-9cf8-4932-a05d-2c5d865d78cc

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