# FDA Inspection 1221019 - Seiler Instrument & Manufacturing Co. Inc. - October 17, 2023

Source: https://www.keypedia.com/records/fda_inspections/seiler-instrument-manufacturing-co-inc/4376a7cf-cf19-45e4-b422-675ea1b610de
Source feed: FDA_Inspections

> FDA Inspection 1221019 for Seiler Instrument & Manufacturing Co. Inc. on October 17, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1221019
- Company Name: Seiler Instrument & Manufacturing Co. Inc.
- Inspection Date: 2023-10-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1221019 - 2023-10-17](https://www.keypedia.com/records/fda_inspections/seiler-instrument-manufacturing-co-inc/925c0265-8ccb-4a48-a09a-60606616c052)
- [FDA Inspection 1029315 - 2017-10-19](https://www.keypedia.com/records/fda_inspections/seiler-instrument-manufacturing-co-inc/c08568f6-34b9-4525-b5e9-61bf0279528c)
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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