# Ocuserv Instruments Inc – FDA Inspection, Oct 15, 2015

Source: https://www.keypedia.com/records/fda_inspections/ocuserv-instruments-inc/7e0fc29e-0271-4a8d-a602-2112762336c8
Source feed: FDA_Inspections

> FDA inspection 945630 of Ocuserv Instruments Inc, October 15, 2015. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 945630
- Company Name: Ocuserv Instruments Inc
- Inspection Date: 2015-10-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 856280 - 2013-11-21
- [FDA Inspection 755236 - 2011-11-21](https://www.keypedia.com/records/fda_inspections/ocuserv-instruments-inc/24dd041e-c1dc-4a89-b659-4b7723c5107a)
- FDA Inspection 601791 - 2009-08-05

Company: https://www.keypedia.com/companies/ocuserv-instruments-inc/4c1718bf-3eae-4bb4-9800-0f60e1c7c284

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