Company
United StatesLisa K. Gidday, M.D., Littleton, CO – FDA Inspections
Inspection records and compliance data for Lisa K. Gidday, M.D. in Littleton, Colorado. 1 FDA inspection on record, last inspected November 09, 2009.
Company Profile
This profile covers Lisa K. Gidday, M.D. based in Littleton, Colorado, United States.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 1
- NAI
- 0
- Form 483s
- 0
- Warning letters
- 0
Inspected November 9, 2009.
Most cited issue areas
- Case history records- inadequate or inadequate1 inspection
- FD-1572, protocol compliance1 inspection
- Safety reports1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| November 9, 2009 | VAI | Human Drugs · Bioresearch Monitoring | 630244 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Lisa K. Gidday, M.D.
FEI Number
3007910623
Address
8199 Southpark Ln Ste 100, Clinical Trial Center of Colorado, Littleton, Colorado 80120, United States
Country
United States
ID: 2c17fbc8-cd1c-42a1-915b-02b1959fbd27