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FDA Inspection
•BizLink Robotic Solutions France•October 31, 2024

FDA Inspection 1254023 - BizLink Robotic Solutions France - October 31, 2024

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Record Details

This FDA Inspection record concerns BizLink Robotic Solutions France, with an inspection on October 31, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
BizLink Robotic Solutions France
Inspection Date
October 31, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Daniel J. Lahar (FDA Associated Person)
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ID · 177cc77f-caf1-4eee-bc7a-8675f7407685

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1254023
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

9
  1. 21 CFR 830.300(a)Devices subject to device identification GUDID data submission requirements.
  2. 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
  3. 21 CFR 820.100(b)Documentation
  4. 21 CFR 820.30(g)Design validation - software validation not performed
  5. 21 CFR 820.50(b)Supplier notification of changes
  6. 21 CFR 820.25(b)Training - Lack of or inadequate procedures
  7. 21 CFR 820.70(g)(2)Periodic equipment inspections
  8. 21 CFR 820.200(a)Servicing - Lack of or inadequate procedures
  9. 21 CFR 820.250(b)Sampling methods - Lack of or inadequate procedures

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