# FDA Inspection 1005167 - Oculo Plastik, Inc. - December 07, 2016

Source: https://www.keypedia.com/records/fda_inspections/oculo-plastik-inc/e21fe4e6-a030-4785-9580-3bc97583fd95
Source feed: FDA_Inspections

> FDA Inspection 1005167 for Oculo Plastik, Inc. on December 07, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005167
- Company Name: Oculo Plastik, Inc.
- Inspection Date: 2016-12-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 941201 - 2015-09-11](https://www.keypedia.com/records/fda_inspections/oculo-plastik-inc/e530a3fd-9ea2-4b01-acc7-04f0710ba77a)
- [FDA Inspection 941201 - 2015-09-11](https://www.keypedia.com/records/fda_inspections/oculo-plastik-inc/819a2033-13c2-4e10-9512-164ebd0b0d81)

Company: https://www.keypedia.com/companies/oculo-plastik-inc/aa18adb3-39c5-4980-861e-81d74020033a

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