FDA Inspection 947314 — PARI Respiratory Equipment, Inc.

PARI Respiratory Equipment, Inc. — FEI 1000142942

The FDA completed an inspection of PARI Respiratory Equipment, Inc. on Nov 3, 2015 in Midlothian, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 3, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Midlothian, VA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
317221 CFR 820.198(c)Investigation of device failures