# FDA Inspection 949785 - Anaerobe Systems - December 01, 2015

Source: https://www.keypedia.com/records/fda_inspections/anaerobe-systems/726fe800-a123-4ed9-ab52-66247d05b5c9
Source feed: FDA_Inspections

> FDA Inspection 949785 for Anaerobe Systems on December 01, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 949785
- Company Name: Anaerobe Systems
- Inspection Date: 2015-12-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 949785 - 2015-12-01](https://www.keypedia.com/records/fda_inspections/anaerobe-systems/c9511306-b7d7-41ca-b6f4-b1a33de6c487)

Company: https://www.keypedia.com/companies/anaerobe-systems/04b2dca1-b398-42a5-9579-5f1ac3dca37d

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