# FDA Inspection 759621 - Hull Anesthesia Inc - December 15, 2011

Source: https://www.keypedia.com/records/fda_inspections/hull-anesthesia-inc/a5ae2d66-c04b-4bc8-b437-0b6bc7c2e827
Source feed: FDA_Inspections

> FDA Inspection 759621 for Hull Anesthesia Inc on December 15, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 759621
- Company Name: Hull Anesthesia Inc
- Inspection Date: 2011-12-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 936031 - 2015-07-27](https://www.keypedia.com/records/fda_inspections/hull-anesthesia-inc/9d64d2a0-bab2-4d07-a22b-07e62219dbd1)
- [FDA Inspection 759621 - 2011-12-15](https://www.keypedia.com/records/fda_inspections/hull-anesthesia-inc/9ff4990a-042f-4b82-8bd4-5c1c243796eb)

Company: https://www.keypedia.com/companies/hull-anesthesia-inc/f2ae10bb-d214-4612-8764-2a6ec2269bd1

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