# FDA Inspection 1089793 - Keeler Instruments Inc - March 18, 2019

Source: https://www.keypedia.com/records/fda_inspections/keeler-instruments-inc/79167886-3b44-48fe-b801-127e653583ea
Source feed: FDA_Inspections

> FDA Inspection 1089793 for Keeler Instruments Inc on March 18, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1089793
- Company Name: Keeler Instruments Inc
- Inspection Date: 2019-03-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/keeler-instruments-inc/5446ce79-8f77-4da7-b449-8c6c1f820013

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