FDA Inspection 725274 — Acorn NMR Inc.

Acorn NMR Inc. — FEI 3004901666

The FDA completed an inspection of Acorn NMR Inc. on May 19, 2011 in Livermore, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 19, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Livermore, CA (United States)

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