# FDA Inspection 801849 - Digitimer Ltd. - August 30, 2012

Source: https://www.keypedia.com/records/fda_inspections/digitimer-ltd/d95a585f-8dad-455f-a213-1fcd493f6bd9
Source feed: FDA_Inspections

> FDA Inspection 801849 for Digitimer Ltd. on August 30, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 801849
- Company Name: Digitimer Ltd.
- Inspection Date: 2012-08-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/digitimer-ltd/fd727190-59d8-4fb8-95ff-fab6028bf5c3

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