# FDA Inspection 855223 - Southeast Aesthetic LTD Co - November 06, 2013

Source: https://www.keypedia.com/records/fda_inspections/southeast-aesthetic-ltd-co/07ed2743-3f6f-41d1-97d8-e7d70f30e6a6
Source feed: FDA_Inspections

> FDA Inspection 855223 for Southeast Aesthetic LTD Co on November 06, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 855223
- Company Name: Southeast Aesthetic LTD Co
- Inspection Date: 2013-11-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 886854 - 2014-07-11](https://www.keypedia.com/records/fda_inspections/southeast-aesthetic-ltd-co/33b870f1-3ead-459e-b50b-b3c6e9b15a1e)
- [FDA Inspection 886854 - 2014-07-11](https://www.keypedia.com/records/fda_inspections/southeast-aesthetic-ltd-co/e16d29c3-97a8-49aa-926c-de9582f64bcf)
- [FDA Inspection 855223 - 2013-11-06](https://www.keypedia.com/records/fda_inspections/southeast-aesthetic-ltd-co/f18c8cd1-64f4-499a-8706-4533264f4ed0)

Company: https://www.keypedia.com/companies/southeast-aesthetic-ltd-co/33d0ff24-eb0a-4b24-ad35-23a27195f406

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