FDA Inspection 1215906 — Bleep, LLC

Bleep, LLC — FEI 3015436853

The FDA completed an inspection of Bleep, LLC on August 25, 2023 in Chapel Hill, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 25, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chapel Hill, NC (United States)

Citations

IDCFRDescription
243021 CFR 820.30(b)Design plans - Lack of or inadequate
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
369621 CFR 820.100(b)Documentation
41921 CFR 820.20(b)Lack of or inadequate organizational structure
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures