# Mannkind Corporation – FDA Inspection, Oct 3, 2024

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

> FDA inspection 1250838 of Mannkind Corporation, October 03, 2024. Classification: No Action Indicated (NAI). 5 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New England District Office
- Citation Count: 5

## Related Documents

- [FDA Inspection 1064802 - 2018-09-07](https://www.keypedia.com/records/fda_inspections/mannkind-corporation/6a902049-a3d3-4fa6-a3c0-f4f6f7c61200)
- FDA Inspection 781626 - 2012-05-15

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sara-m-onyango/643c6ad3-9747-4bc2-9e8e-72f97b11e659)

Company: https://www.keypedia.com/companies/mannkind-corporation/c4fe67e8-1e0c-48fb-9847-e8a284409d8c

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