# FDA Inspection 1029315 - Seiler Instrument & Manufacturing Co. Inc. - October 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/seiler-instrument-manufacturing-co-inc/c08568f6-34b9-4525-b5e9-61bf0279528c
Source feed: FDA_Inspections

> FDA Inspection 1029315 for Seiler Instrument & Manufacturing Co. Inc. on October 19, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029315
- Company Name: Seiler Instrument & Manufacturing Co. Inc.
- Inspection Date: 2017-10-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/seiler-instrument-manufacturing-co-inc/4197384c-d9c0-4a6c-9fc2-1dbff5710c47

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