# Mannkind Corporation – FDA Inspection, Sep 7, 2018

Source: https://www.keypedia.com/records/fda_inspections/mannkind-corporation/6a902049-a3d3-4fa6-a3c0-f4f6f7c61200
Source feed: FDA_Inspections

> FDA inspection 1064802 of Mannkind Corporation, September 07, 2018. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064802
- Company Name: Mannkind Corporation
- Inspection Date: 2018-09-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1250838 - 2024-10-03](https://www.keypedia.com/records/fda_inspections/mannkind-corporation/84d9c0c9-a0a3-4c10-a79e-d4dc764bc005)
- FDA Inspection 781626 - 2012-05-15

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nabil-nakhoul/d676e9c9-566c-4e59-84e8-1dc474e4e48d)

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

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