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

Source: https://www.globalkeysolutions.net/records/fda_inspections/mannkind-corporation/84d9c0c9-a0a3-4c10-a79e-d4dc764bc005
Source feed: FDA_Inspections

> FDA Inspection 1250838 for Mannkind Corporation on October 03, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1250838
- Company Name: Mannkind Corporation
- Inspection Date: 2024-10-03
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New England District Office

## Related Documents

- [FDA Inspection 1250838 - 2024-10-03](https://www.globalkeysolutions.net/records/fda_inspections/mannkind-corporation/e60239b9-143a-4b9a-a19a-784974994e10)
- [FDA Inspection 1250838 - 2024-10-03](https://www.globalkeysolutions.net/records/fda_inspections/mannkind-corporation/72a438f7-9e6b-48f9-8a9a-c6f1b4abb883)
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Company: https://www.globalkeysolutions.net/companies/mannkind-corporation/c4fe67e8-1e0c-48fb-9847-e8a284409d8c

Office: https://www.globalkeysolutions.net/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144