# FDA Inspection 1014973 - Nidek Technologies SRL - May 03, 2017

Source: https://www.keypedia.com/records/fda_inspections/nidek-technologies-srl/f5931d2a-3a36-4d06-8ca3-134ea46a8e30
Source feed: FDA_Inspections

> FDA Inspection 1014973 for Nidek Technologies SRL on May 03, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014973
- Company Name: Nidek Technologies SRL
- Inspection Date: 2017-05-03
- 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 1014973 - 2017-05-03](https://www.keypedia.com/records/fda_inspections/nidek-technologies-srl/e54df6b9-491a-46b1-b840-4b4b293f0d2c)

Company: https://www.keypedia.com/companies/nidek-technologies-srl/16dbcd0c-8a6b-40a9-959b-4cd1e52dd926

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