# FDA Inspection 1006523 - Coopervision Manufacturing, Ltd - January 19, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/coopervision-manufacturing-ltd/83911168-474f-477b-a748-9889588e816a
Source feed: FDA_Inspections

> FDA Inspection 1006523 for Coopervision Manufacturing, Ltd on January 19, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1006523
- Company Name: Coopervision Manufacturing, Ltd
- Inspection Date: 2017-01-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1079354 - 2019-01-17](https://www.globalkeysolutions.net/records/fda_inspections/coopervision-manufacturing-ltd/9da420fc-813b-4fba-accb-cce158c5b840)
- [FDA Inspection 859895 - 2013-12-05](https://www.globalkeysolutions.net/records/fda_inspections/coopervision-manufacturing-ltd/b598e19a-86ae-4684-bf96-96ab3631ef90)

Company: https://www.globalkeysolutions.net/companies/coopervision-manufacturing-ltd/364600de-7712-44eb-a131-78eaf65112eb

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