FDA Inspection 1192743 — Johnson Medtech LLC

Johnson Medtech LLC — FEI 3013522941

The FDA completed an inspection of Johnson Medtech LLC on December 8, 2022 in Vandalia, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 8, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Vandalia, OH (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
316021 CFR 820.184Lack of or inadequate DHR procedures
326621 CFR 820.86Acceptance status
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
53721 CFR 820.70(a)Production processes
54621 CFR 820.75(a)Lack of or inadequate process validation