FDA Inspection 1016324 — Christopher P. Recknor MD

Christopher P. Recknor MD — FEI 3007874189

The FDA completed an inspection of Christopher P. Recknor MD on May 1, 2017 in Gainesville, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 1, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Gainesville, GA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
722721 CFR 50.27(a)Consent form not approved/signed/dated
753021 CFR 312.62(b)Case history records- inadequate or inadequate