# FDA Inspection 1026884 - Welmed Inc. - August 30, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/welmed-inc/41364eae-92f4-41c5-8655-d8c6f1abb31a
Source feed: FDA_Inspections

> FDA Inspection 1026884 for Welmed Inc. on August 30, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026884
- Company Name: Welmed Inc.
- Inspection Date: 2017-08-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/welmed-inc/778f4417-f6f6-466b-97e7-3cde8e60ac5b

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