# FDA Inspection 926321 - Anbotek Compliance Laboratory Ltd. - November 06, 2014

Source: https://www.keypedia.com/records/fda_inspections/anbotek-compliance-laboratory-ltd/52f68401-1a2d-4f10-abe7-d08a9f6cb6e5
Source feed: FDA_Inspections

> FDA Inspection 926321 for Anbotek Compliance Laboratory Ltd. on November 06, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 926321
- Company Name: Anbotek Compliance Laboratory Ltd.
- Inspection Date: 2014-11-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/anbotek-compliance-laboratory-ltd/9f32b9a0-9f2c-4900-8bb7-e6c4df6ced55

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