# FDA Inspection 993003 - Pulmonx, Corp. - November 08, 2016

Source: https://www.keypedia.com/records/fda_inspections/pulmonx-corp/3595a533-63f7-40c5-9261-027eeaad19dd
Source feed: FDA_Inspections

> FDA Inspection 993003 for Pulmonx, Corp. on November 08, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993003
- Company Name: Pulmonx, Corp.
- Inspection Date: 2016-11-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 993003 - 2016-11-08](https://www.keypedia.com/records/fda_inspections/pulmonx-corp/ec2f0407-d0d0-4182-90c2-49a70d591c9d)
- [FDA Inspection 862529 - 2014-02-21](https://www.keypedia.com/records/fda_inspections/pulmonx-corp/8be320de-6088-4657-89d0-bb14bf335558)
- [FDA Inspection 862529 - 2014-02-21](https://www.keypedia.com/records/fda_inspections/pulmonx-corp/c06bf2b9-3410-41da-8246-b769d44e7afa)

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