FDA Inspection 803882 — KVK Tech, Inc.
The FDA completed an inspection of KVK Tech, Inc. on Sep 17, 2012 in Newtown, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 17, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Newtown, PA (United States)
Additional Details
Postmarket Adverse Drug Experience (PADE)