# FDA Inspection 936721 - Sklar Instruments - August 03, 2015

Source: https://www.keypedia.com/records/fda_inspections/sklar-instruments/601f600c-27bc-40d2-8fe4-849db5e82625
Source feed: FDA_Inspections

> FDA Inspection 936721 for Sklar Instruments on August 03, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 936721
- Company Name: Sklar Instruments
- Inspection Date: 2015-08-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 936721 - 2015-08-03](https://www.keypedia.com/records/fda_inspections/sklar-instruments/5eff4ce4-728b-46c1-a23b-c6d21a505b31)
- [FDA Inspection 747975 - 2011-09-30](https://www.keypedia.com/records/fda_inspections/sklar-instruments/0b362f0e-0797-4fe3-be9a-8bb107320777)

Company: https://www.keypedia.com/companies/sklar-instruments/8afc7560-be77-4f92-aa4b-daedabfd5c1b

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