# FDA Inspection 1020101 - OphthalMed LLC - May 01, 2017

Source: https://www.keypedia.com/records/fda_inspections/ophthalmed-llc/41e7f783-6438-4102-aef7-455476cd9dcc
Source feed: FDA_Inspections

> FDA Inspection 1020101 for OphthalMed LLC on May 01, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020101
- Company Name: OphthalMed LLC
- Inspection Date: 2017-05-01
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1020101 - 2017-05-01](https://www.keypedia.com/records/fda_inspections/ophthalmed-llc/774593e4-8a31-4a55-a347-9ab2282c2463)
- [FDA Inspection 868674 - 2014-02-24](https://www.keypedia.com/records/fda_inspections/ophthalmed-llc/725c8010-7392-49ee-9408-119b04e7d89f)
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- [FDA Inspection 739449 - 2011-08-02](https://www.keypedia.com/records/fda_inspections/ophthalmed-llc/86d1d883-5a15-42d8-b621-57836cabbc3a)

Company: https://www.keypedia.com/companies/ophthalmed-llc/453bb21e-f8be-4a90-820c-4a5741c80861

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