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  2. Glossary
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  3. NAI

NAI

No action indicated (NAI) means no objectionable conditions or practices were found during the inspection. No FDA form 483 is issued for an NAI outcome inspection.

Data Sources
FDA Inspection Classifications Database
FDA Inspections / 483 Database Search
FDA MAUDE database
ORA FOIA Electronic Reading Room
Health Agencies & Organizations
ANVISA
CBER
CDER
CDRH
Cofepris
EMA
FDA
HSA
Health Canada
ISO
MFDS
MHRA
MedSafe
NMPA
ORA
PMDA
Pharmac
Swissmedic
TGA
WHO
Data Sources
21 CFR 820.30
483
483R
510k
ALCOA, ALCOA+, AND ALCOA++
API
Application-Based Inspection
BLA
Biosimilar
CAPA (Corrective and Preventive Action)
CFR
CGT
CQAs
CRL
Citation
Clinical Trial
Close out letter
Cross-Contamination
Data Integrity
Deficiency
Design Controls
Drug Recall
Drug Shortage
EIR
Excipient
FDA 483 Observation
FDF
FEI
FOIA
Federal Register
Follow-up Inspections
For-cause Inspection
GCP
GDP
GLP
GVP
GxP
ICH Q9
Import Alert
Inspection Types
Inspection outcome classifications
Legacy Product
MRA
Modality
NDA
OAI
PAI
PLI
PMA
PMS
Pharmacopeia
Quality Compliance
Quality Systems
Routine Inspection
SOP
Surveillance Inspection
Terminated Recall
Untitled Letter
VAI
Warning Letter
[C]GMP
Redica Systems Terms
Clinical Strategy
Criticality/Severity
DocIQ™
Inferred Observation / Citation
Inspection Intelligence
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Premarket Intelligence
Quality System Labeling
Quality Unit Intelligence
Red Flag Models
Redica AI Agents
Redica ID™
Redica Ontologies
Regulatory Intelligence
Site Risk Score™
Vendor Intelligence
Vendor Risk Score™

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