# FDA Inspection 1192167 - Gulden Ophthalmics - October 27, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/gulden-ophthalmics/fc1dd314-8352-4780-a5f8-2d60dba57c3b/
Source feed: FDA_Inspections

> FDA Inspection 1192167 for Gulden Ophthalmics on October 27, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1192167
- Company Name: Gulden Ophthalmics
- Inspection Date: 2022-10-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1192167 - 2022-10-27](https://www.globalkeysolutions.net/api/records/fda_inspections/gulden-ophthalmics/e44ccf8f-c2b3-44fe-b151-7291b534e769/)
- [FDA Inspection 1084158 - 2019-03-14](https://www.globalkeysolutions.net/api/records/fda_inspections/gulden-ophthalmics/3e8ce10b-d71c-47a1-9482-c96e37b7fd37/)
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- [FDA Inspection 647322 - 2010-01-27](https://www.globalkeysolutions.net/api/records/fda_inspections/gulden-ophthalmics/3c62531a-1ba2-4440-bb2c-eb74928daa13/)
- [FDA Inspection 647322 - 2010-01-27](https://www.globalkeysolutions.net/api/records/fda_inspections/gulden-ophthalmics/90a72e35-5f4d-4b4c-b74e-0f4313f8f788/)

Company: https://www.globalkeysolutions.net/companies/gulden-ophthalmics/2c5e3f13-df76-4137-9624-029df943cdcc

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