FDA Inspection 723490 — Synchpack Inc.

Synchpack Inc. — FEI 3004535074

The FDA completed an inspection of Synchpack Inc. on May 6, 2011 in Maple Grove, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 6 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 6, 2011
Fiscal Year
2011
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Maple Grove, MN (United States)

Citations

IDCFRDescription
1568321 CFR 111.315(c)Examination, testing methods; criteria for selecting
1584721 CFR 111.73Specifications met - component identity
1586921 CFR 111.75(c)Specifications met - verify; finished batch
1592821 CFR 111.103Written procedure quality control operations material review
1595121 CFR 111.110(c)Quality control operations - tests, examinations; results
1597821 CFR 111.123(a)(2)Quality control operations - batch production records