# Boekel Scientific – FDA Inspection, Mar 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/boekel-scientific/ee44b1f8-17ab-4947-9bd3-b029ad76ab0a
Source feed: FDA_Inspections

> FDA inspection 1005517 of Boekel Scientific, March 10, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005517
- Company Name: Boekel Scientific
- Inspection Date: 2017-03-10
- 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: 1

## Related Documents

- FDA Inspection 1237714 - 2024-04-18

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brian-s-keefer/4fec578b-ca72-4d79-8634-3a9fe7ecd9a5)

Company: https://www.keypedia.com/companies/boekel-scientific/1a5d4cd5-edec-4748-bbca-332caea57468

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