# FDA Inspection 989790 - Dutch Ophthalmic USA, Inc. - October 24, 2016

Source: https://www.keypedia.com/records/fda_inspections/dutch-ophthalmic-usa-inc/d0cd3dab-ee0e-4131-adbb-e7205f9f53f5
Source feed: FDA_Inspections

> FDA Inspection 989790 for Dutch Ophthalmic USA, Inc. on October 24, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989790
- Company Name: Dutch Ophthalmic USA, Inc.
- Inspection Date: 2016-10-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 727303 - 2011-06-03](https://www.keypedia.com/records/fda_inspections/dutch-ophthalmic-usa-inc/4460b1ee-f922-4e32-b47b-4c0637f2df11)
- [FDA Inspection 727303 - 2011-06-03](https://www.keypedia.com/records/fda_inspections/dutch-ophthalmic-usa-inc/3ac3b7e7-eddd-46e0-a031-9969da056aab)
- [FDA Inspection 727303 - 2011-06-03](https://www.keypedia.com/records/fda_inspections/dutch-ophthalmic-usa-inc/4b2872ef-64e8-45e5-bdfa-42ee6db1b4d2)

Company: https://www.keypedia.com/companies/dutch-ophthalmic-usa-inc/6367eefb-d3d2-49b9-9a8e-36ddfdbfca10

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