FDA Inspection 907533 — Sgarlato Med, LLC

Sgarlato Med, LLC — FEI 2939320

The FDA completed an inspection of Sgarlato Med, LLC on December 19, 2014 in San Jose, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 15 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 19, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Jose, CA (United States)

Citations

IDCFRDescription
1471121 CFR 820.160(a)Lack of or inadequate procedures for distribution
1472021 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
1472221 CFR 820.40Procedures not adequately established or maintained
226921 CFR 820.20(a)Quality policy and objectives
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
310421 CFR 820.30(j)Design history file
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
316021 CFR 820.184Lack of or inadequate DHR procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
333121 CFR 820.181DMR - not or inadequately maintained
341521 CFR 820.22Quality Audit/Reaudit - conducted
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency
367121 CFR 820.25(a)Personnel
41921 CFR 820.20(b)Lack of or inadequate organizational structure