# FDA Inspection 1250838 - Mannkind Corporation - October 03, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/mannkind-corporation/72a438f7-9e6b-48f9-8a9a-c6f1b4abb883
Source feed: FDA_Inspections

> FDA Inspection 1250838 for Mannkind Corporation on October 03, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1250838
- Company Name: Mannkind Corporation
- Inspection Date: 2024-10-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1250838 - 2024-10-03](https://www.globalkeysolutions.net/records/fda_inspections/mannkind-corporation/84d9c0c9-a0a3-4c10-a79e-d4dc764bc005)
- [FDA Inspection 1250838 - 2024-10-03](https://www.globalkeysolutions.net/records/fda_inspections/mannkind-corporation/e60239b9-143a-4b9a-a19a-784974994e10)
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Company: https://www.globalkeysolutions.net/companies/mannkind-corporation/c4fe67e8-1e0c-48fb-9847-e8a284409d8c

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