FDA Inspection
Hittech Multin B.VHittech Multin B.V – FDA Inspection, May 31, 2017
Record Details
This FDA Inspection record concerns Hittech Multin B.V, with an inspection on May 31, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · a6d80840-5420-4dae-99fe-da990a22f8d5
Inspection Facts
- Inspection number
- 1012683
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.20(c)Management review - Lack of or inadequate procedures
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
- 21 CFR 820.72(a)Equipment control activity documentation
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