# FDA Inspection 993577 - Porta-lung Company - November 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/porta-lung-company/d5972cc3-0d54-46fb-8b6c-a14e7497fd93
Source feed: FDA_Inspections

> FDA Inspection 993577 for Porta-lung Company on November 29, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993577
- Company Name: Porta-lung Company
- Inspection Date: 2016-11-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/porta-lung-company/1d0aa5b6-df4d-4992-9e05-9aeb807a77cc

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