# Pulmonx, Corp. – FDA Inspection, Nov 8, 2016

Source: https://www.keypedia.com/records/fda_inspections/pulmonx-corp/ec2f0407-d0d0-4182-90c2-49a70d591c9d
Source feed: FDA_Inspections

> FDA inspection 993003 of Pulmonx, Corp., November 08, 2016. Classification: No Action Indicated (NAI). 2 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: 993003
- Company Name: Pulmonx, Corp.
- Inspection Date: 2016-11-08
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

Company: https://www.keypedia.com/companies/pulmonx-corp/af48a2eb-bb34-4213-9d1e-32302208331a

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