# FDA Inspection 1008948 - Ophtec BV - March 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/ophtec-bv/4af7d630-b354-413f-8e73-374a73830b97
Source feed: FDA_Inspections

> FDA Inspection 1008948 for Ophtec BV on March 23, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008948
- Company Name: Ophtec BV
- Inspection Date: 2017-03-23
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1008948 - 2017-03-23](https://www.keypedia.com/records/fda_inspections/ophtec-bv/6e8dce30-f0ab-4600-84a4-3b5d547399a3)

Company: https://www.keypedia.com/companies/ophtec-bv/c9991327-93c8-4e2b-b443-62f4e5f81d71

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