# FDA Inspection 680312 - Anulex Technologies Inc - September 22, 2010

Source: https://www.keypedia.com/records/fda_inspections/anulex-technologies-inc/42cbf0c9-fa29-47c0-875a-ffed09eef1b1
Source feed: FDA_Inspections

> FDA Inspection 680312 for Anulex Technologies Inc on September 22, 2010. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 680312
- Company Name: Anulex Technologies Inc
- Inspection Date: 2010-09-22
- Classification: Official Action Indicated (OAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 835254 - 2013-05-06](https://www.keypedia.com/records/fda_inspections/anulex-technologies-inc/b132c6d1-9dfe-4941-a7ad-f651d038ab48)
- [FDA Inspection 656148 - 2010-04-08](https://www.keypedia.com/records/fda_inspections/anulex-technologies-inc/ced53605-9969-4c90-bd32-68993e43f7c0)

Company: https://www.keypedia.com/companies/anulex-technologies-inc/3eacaf53-2188-43f9-93be-e99a512be2e6

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