FDA Inspection
Boekel ScientificBoekel Scientific – FDA Inspection, Mar 10, 2017
Record Details
This FDA Inspection record concerns Boekel Scientific, with an inspection on March 10, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ee44b1f8-17ab-4947-9bd3-b029ad76ab0a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1005517
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
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Other FDA inspections of Boekel Scientific
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 18, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Boekel Scientific
- FDA Inspection 1237714 - 2024-04-18
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