FDA Inspection 1034036 — Tolmar, Inc.

Tolmar, Inc. — FEI 3006218434

The FDA completed an inspection of Tolmar, Inc. on December 6, 2017 in Fort Collins, CO. 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
December 6, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Fort Collins, CO (United States)

Citations

IDCFRDescription
126321 CFR 211.68(b)Computer control of master formula records
431421 CFR 211.84(d)(2)Reports of Analysis (Components)