FDA Inspection 797078 — R.W.K., Inc.

R.W.K., Inc. — FEI 1000116367

The FDA completed an inspection of R.W.K., Inc. on Aug 17, 2012 in Albert Lea, MN. 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
Aug 17, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Albert Lea, MN (United States)