FDA Inspection 1208562 — CoRE labs, LLC

CoRE labs, LLC — FEI 3001620005

The FDA completed an inspection of CoRE labs, LLC on June 21, 2023 in Englewood, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 21, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Englewood, CO (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1472221 CFR 820.40Procedures not adequately established or maintained
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures