# FDA Inspection 934935 - Digitimer Ltd. - July 02, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/digitimer-ltd/9b439e9c-d06c-4e73-b5b1-b627779d6cca
Source feed: FDA_Inspections

> FDA Inspection 934935 for Digitimer Ltd. on July 02, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 934935
- Company Name: Digitimer Ltd.
- Inspection Date: 2015-07-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 934935 - 2015-07-02](https://www.globalkeysolutions.net/records/fda_inspections/digitimer-ltd/dfe717da-e796-496c-aa54-17f18520d4e3)
- [FDA Inspection 801849 - 2012-08-30](https://www.globalkeysolutions.net/records/fda_inspections/digitimer-ltd/d95a585f-8dad-455f-a213-1fcd493f6bd9)

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

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