# Seiler Instrument & Manufacturing Co. Inc. – FDA Inspection, Oct 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 of Seiler Instrument & Manufacturing Co. Inc., October 19, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- 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 1221019 - 2023-10-17

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)

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