FDA Inspection 1066940 — KVK Tech, Inc.
The FDA completed an inspection of KVK Tech, Inc. on September 21, 2018 in Newtown, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 21, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Newtown, PA (United States)
Additional Details
Postmarket Adverse Drug Experience (PADE)