FDA Inspection 1082260 — Turbett Surgical, Inc.

Turbett Surgical, Inc. — FEI 3012421755

The FDA completed an inspection of Turbett Surgical, Inc. on March 6, 2019 in Henrietta, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 6, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Henrietta, NY (United States)

Citations

IDCFRDescription
1471421 CFR 820.30(c)Design input - Lack of or inadequate procedures
1471521 CFR 820.30(d)Design output - Lack of or inadequate procedures
310221 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures