# FDA Inspection 727303 - Dutch Ophthalmic USA, Inc. - June 03, 2011

Source: https://www.keypedia.com/records/fda_inspections/dutch-ophthalmic-usa-inc/4b2872ef-64e8-45e5-bdfa-42ee6db1b4d2
Source feed: FDA_Inspections

> FDA Inspection 727303 for Dutch Ophthalmic USA, Inc. on June 03, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 727303
- Company Name: Dutch Ophthalmic USA, Inc.
- Inspection Date: 2011-06-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 989790 - 2016-10-24](https://www.keypedia.com/records/fda_inspections/dutch-ophthalmic-usa-inc/d0cd3dab-ee0e-4131-adbb-e7205f9f53f5)
- [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)

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