FDA Inspection 754500 — Reichert, Inc.

Reichert, Inc. — FEI 1000159913

The FDA completed an inspection of Reichert, Inc. on November 22, 2011 in Depew, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 22, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Depew, NY (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
317021 CFR 820.198(b)Review and evaluation for investigation