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FDA Inspection
•Stoll Metalcraft Inc•October 11, 2023

Stoll Metalcraft Inc – FDA Inspection, Oct 11, 2023

Record Details

This FDA Inspection record concerns Stoll Metalcraft Inc, with an inspection on October 11, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Stoll Metalcraft Inc
Inspection Date
October 11, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Kelvin Cheung (Issuing Officer)
View Company Profile

ID · a50b0bc7-78bb-4748-92a2-b92228a8a699

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1220159
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.184DHR content
  2. 21 CFR 820.72(b)Remedial action - documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Stoll Metalcraft Inc

1
DateClassificationOfficeProject area
December 4, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Stoll Metalcraft Inc
  • FDA Inspection 857765 - 2013-12-04

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